Bioartificial liver support systems for acute liver failure: A systematic review and meta-analysis of the clinical and preclinical literature

Abstract

BACKGROUND

Acute liver failure (ALF) has a high mortality varying from 80% to 85% with rapid progress in multi-organ system failure. Bioartificial liver (BAL) support systems have the potential to provide temporary support to bridge patients with ALF to liver transplantation or spontaneous recovery. In the past decades, several BAL support systems have been conducted in clinical trials. More recently, concerns have been raised on the renovation of high-quality cell sources and configuration of BAL support systems to provide more benefits to ALF models in preclinical experiments.

AIM

To investigate the characteristics of studies about BAL support systems for ALF, and to evaluate their effects on mortality.

METHODS

Eligible clinical trials and preclinical experiments on large animals were identified on Cochrane Library, PubMed, and EMbase up to March 6, 2019. Two reviewers independently extracted the necessary information, including key BAL indicators, survival and indicating outcomes, and adverse events during treatment. Descriptive analysis was used to identify the characteristics of the included studies, and a meta-analysis including only randomized controlled trial (RCT) studies was done to calculate the overall effect of BAL on mortality among humans and large animals, respectively.

RESULTS

Of the 30 selected studies, 18 were clinical trials and 12 were preclinical experiments. The meta-analysis result suggested that BAL might reduce mortality in ALF in large animals, probably due to the recent improvement of BAL, including the type, cell source, cell mass, and bioreactor, but seemed ineffective for humans [BAL vs control: relative risk (95% confidence interval), 0.27 (0.12-0.62) for animals and 0.72 (0.48-1.08) for humans]. Liver and renal functions, hematologic and coagulative parameters, encephalopathy index, and neurological indicators seemed to improve after BAL, with neither meaningful adverse events nor porcine endogenous retrovirus infection.

CONCLUSION

BAL may reduce the mortality of ALF by bridging the gap between preclinical experiments and clinical trials. Clinical trials using improved BAL must be designed scientifically and conducted in the future to provide evidence for transformation.

Key Words: Bioartificial liver; Acute liver failure; Preclinical experiment; Clinical trial; Meta-analysis

Core tip: This systematic review and meta-analysis included a large number of studies about clinical trials and preclinical experiments of bioartificial liver (BAL) support systems for treating patients and large animal models with acute liver failure. We summarized the characteristics of studies, BAL, and outcomes in all the studies and compared the pooled effect by meta-analysis including only randomized controlled trial studies regarding mortality after BAL among humans and large animals, respectively.

INTRODUCTION

Acute liver failure (ALF) is characterized by an acute episode of liver dysfunction in individuals without underlying chronic liver diseases, sometimes causing a rapid onset of encephalopathy and coagulopathy followed by multiorgan system failure. Patients with ALF have a high mortality ranging from 80% to 85%, approaching 90% among those with severe fulminant hepatic failure (FHF)[1]. The most effective treatment method for patients with ALF is liver transplantation, as it has increased the 5-year survival rate by 75%[2]. Although some patients might recover spontaneously, many would die during waiting for a compatible donor because of aggressive deterioration of liver function or development of cerebral edema, intracranial hypertension, and even irreversible brain damage. Thus, a liver support system must be developed to maintain a viable status of these patients prior to the transplantation.

During the past decades, several artificial devices for removing toxins from patients’ blood through filtration and adsorption have improved clinical status in some cases. However, a meta-analysis of six randomized controlled trials (RCTs) concluded that artificial liver support systems might not reduce the mortality in ALF[3]. Moreover, the newly developed bioartificial liver (BAL) support systems that incorporate a hepatoma cell line or primary hepatocytes into a bioreactor when processing blood or plasma proved meaningful for prolonging the survival time of ALF animals in preclinical trials. Several types have been applied for the treatment of patients with ALF in phase I studies or controlled clinical trials, and improved neurological status and liver and renal functions, thus bridging to transplantation or spontaneous recovery[4-7]. However, the survival outcome and adverse effects of such alternative methods are controversial[3,8].

In addition, the BAL has various types with different cell sources, cell mass, and culture methods, as well as architectural design such as the bioreactor, scaffold, and separation, which might be associated with the effect and safety of the BAL in treating ALF[9]. Furthermore, the BAL has been modified and renovated in preclinical experiments on large animals but has not been used in clinical trials[10-12], which caused a significant gap between clinical and preclinical studies.

One objective of our study was to investigate the characteristics of studies about BAL for ALF in both clinical trials and recent preclinical experiments on large animals. In particular, we looked at key indicators of the BAL, survival outcome, and adverse events regarding the treatment. Another objective was to evaluate the pooled effect of the BAL on mortality by conducting a meta-analysis of randomized controlled studies stratified among patients with ALF and large animals.

MATERIALS AND METHODS

This study was constructed following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. The protocol has been registered in PROSPERO, an international prospective register of systematic reviews (Registration number: CRD42019133215).

Inclusion and exclusion criteria

We included studies about any of the BAL for ALF, including all clinical trials, case reports, and RCTs in patients with ALF and preclinical experiments in large animals (monkeys, pigs, and dogs) published in the past 10 years. The language was limited to English.

The exclusion criteria were as follows: (1) Not focusing on the outcome of BAL, or the ALF group could not be separated from the other study populations such as patients with acute-on-chronic liver failure; (2) Duplicates of previous publications; (3) Based on incomplete data; and (4) Reviews, meta-analyses, comments, guidelines, letters, editorial articles, and project or conference summaries. If more than one study by the same author using the same data was published, either the study with the largest sample size or the most recently published study was included.

Literature search and selection

By using a searching strategy and filter that combined keywords or subjects about BAL and ALF, which had been pre-tested and improved repeatedly, we searched the Cochrane Library, PubMed, and EMbase to identify eligible articles till March 6, 2019 according to the inclusion and exclusion criteria, by setting the following key elements (Patients: ALF; Intervention: BAL; Comparison: None; Outcome: including but not limited to mortality, bridging time, liver and renal function; keywords used for literature search are shown in Supplementary-material). Literature about preclinical experiments in large animals was limited to papers published in the past 10 years. The references used in the eligible articles were also reviewed to examine other potential sources.

Teams of paired reviewers who were trained and knowledgeable about the study screened the literature independently. We screened the title and keywords first and excluded unqualified studies according to the predefined criteria. Then, we read the abstracts and full texts carefully to further exclude unqualified literature. The decision to exclude studies was determined by two reviewers. Inconsistent results were resolved either by discussion or decided by a third reviewer. Finally, the remaining studies were enrolled to be reviewed and analyzed. The flow chart of the study selection is shown in Figure 1.

Figure 1 Flow chart of study selection.

Data extraction

We extracted the following information from each eligible article: (1) basic information of the included studies, including the publication year, title of the article, journal along with impact factor in 2018, country of the first author, study setting, study type (clinical trial, case report, or preclinical experiment), and data sources (full text and abstract); (2) detailed information of clinical trials in humans, including the type of BAL [e.g., HepatAssist, extracorporeal liver assist device (ELAD), academic medical center (AMC)-BAL, modular extracorporeal liver support (MELS), novel bioartificial liver support system (BLSS), radial-flow bioreactor (RFB)-BAL, and hybrid bioartificial liver (HBAL)], whether hybrid or not, cell sources (e.g., porcine hepatocytes, C3A cells, or primary human hepatocytes), cell mass, sample size, ALF subtype [fulminant hepatic failure (FHF) or primary nonfunction (PNF)], age and sex of subjects, disease etiology [e.g., PNF, viral, indeterminate, autoimmune, Acetaminophen (AO), and ischemic], BAL treatment time, outcomes (i.e., bridging time, orthotopic liver transplantation, death events, and recovery), follow-up time, stable or unstable hemodynamics, effects on liver and renal functions, hematologic and coagulative parameters, encephalopathy index, neurological status, adverse events during treatment (e.g., transitory hypotension), and porcine endogenous retrovirus (PERV) test result; (3) data of preclinical experiment on large animals, including animal species (e.g., pig, canine, and monkey), number of animals, sex (female and male), weight (kg), inducer of acute liver failure (e.g., D-galactosamine, hepatic artery ligation, surgical ligation of all blood flow to the liver, α-amanitin, and lipopolysaccharide), type of BAL (e.g., FBBAL, HBAL, HBALSS, SRBAL, hiHep-BAL, and UCLBAL), cell sources (e.g., alginate-chitosan encapsulated primary porcine hepatocytes, co-cultured pig hepatocytes, bone marrow mesenchymal stem cells, human hepatic CL-1 cells grown in microgravity culture, HiHeps, and three-dimensional HepG2-cell spheroids), cell mass, bioreactor (e.g., choanoid fluidized bed bioreactor, multi-layer flat-plate bioreactor anionic resin adsorption column, fluidized-bed bioreactor, perfusion bioreactor, spheroid reservoir, and packed-bed bioreactor), treatment time, survival time or rate at a specific time point, other effects such as ammonia level, and PERV test result.

For data extraction and scoring, paired reviewers conducted the survey independently on the basis of the literature database and recorded the necessary information. The results of the paired reviewers were cross-checked, and disagreements were resolved by discussion or decided by a third reviewer.

Statistical analysis

We conducted description analyses of the study characteristics of clinical trials and preclinical experiments on large animals by using the absolute numbers and percentages of the qualitative variables, and mean [standard deviation (SD)] or median (percentile) of the quantitative data. The bias risk of the included RCT studies was assessed according to the Cochrane assessment method for RCTs, while risk of non-RCT studies was assessed according to the Newcastle-Ottawa Quality Assessment Scale for cohort studies.

By selecting clinical RCTs and preclinical RCT experiments with survival outcome (death event) recorded at a specific time, we combined the effect of selected studies on the relative ratio (RR) scale by performing a meta-analysis with a random effect model and assigning weights according to the estimated variance. The heterogeneity of the included studies was also tested, with Q-test significance (P < 0.05) or I² > 50% indicating that heterogeneity existed between studies. The overall RR and 95% confidence interval (CI) were calculated. We also conducted sensitivity analyses to examine the impact of using alternative effect measures (odds ratio vs relative ratio), pooling methods [Peto vs Mantel-Hanszel (M-H)], and statistical models (fixed- vs random-effects). Begg’s funnel plot was also used to evaluate the publication bias.

All the statistical analyses were performed with SPSS 23.0 (IBM Corp. Armonk, NY, United States) and Review Manager 5.3 (RevMan, the Cochrane Collaboration, Oxford, England).

RESULTS

We identified 215 studies preliminarily, and then excluded 67 unrelated or ineligible articles, 34 articles about artificial liver support system, 14 articles about in vitro function evaluation, 1 duplicate article, 4 articles with unavailable data, and 65 reviews. We finally included 30 articles in the analyses, of which 18 were human clinical trials[6,7,13-28] (only 2 were RCT studies[6,7]) and 12 were preclinical experiments in large animals[5,10-12,29-36].

Among the 30 articles, 94.4% (17/18) were clinical trials published before 2005, with only 1 phase I clinical trial published in 2018 (only abstract available). Studies about preclinical experiments in large animals in the recent 10 years accounted for 40% of the articles (12/30). The median (P₂₅-P₇₅) impact factor (IF) of the journals was 4.04 (2.60-9.20), with 8 articles having an IF < 3 and 5 having an IF > 10. Approximately two-thirds of the studies were conducted by authors in the United States (11/30) and China (8/30). One RCT study was done in England and published in Hepatology in 1996[7] while the other one was performed in 11 United States and 9 European sites by United States researchers and published in Annals of Surgery in 2004[6]. More than one-third (12/30) of the studies were about hybrid support systems (e.g., HBAL, MELS, HBALSS, and HepatAssist), distributed in 9 clinical trial studies and 3 preclinical experimental studies. The available data that we analyzed were mostly from full texts (29/30), and 1 abstract of clinical trial was also included considering the limited number of eligible studies in humans and the availability of valuable information in the abstract (as shown in Supplemental Table 1).

Table 1 Characteristics of bioartificial liver support system and subjects of clinical trials.

ID	Publication year	Type of trial	BAL system				Subject
			Type	Hybrid	Cell	Mass	Sample No.	Subtype	Age	Sex	Disease etiology
1	1994	Non-controlled trial	HepatAssist	Yes	Porcine hepatocytes	6 × 109	7	FHF 6 PNF 1	10-58	4M:3F	PNF 1 ; Virus 1; AO 2; Indeterminate 3
2	1997	Non-controlled trial	HepatAssist	Yes	Porcine hepatocytes	5 × 109	21	FHF 18	36.1 ± 3.4	7M:11F	Virus 4; Indeterminate 8; AO 4; Ischemic 2
								PNF 3	48.3 ± 11.2	1M:2F	Virus 1; Indeterminate 1; Autoimmune 1
3	2010	Non-controlled trial	HepatAssist	Yes	Porcine hepatocytes	5 × 109	18	FHF 15	10-56	10M;5F	Indeterminate 7; Virus 3; AO 4; Ischemic 1
								PNF 3	26-58	1M:2F	Indeterminate 1; Virus 1; Autoimmune 1;
4	2002	Non-controlled trial	HepatAssist	Yes	Porcine hepatocytes	5 × 109	10	FHF 10	31	4M:6F	Indeterminate 6; Virus 2; Wilson 1; Pyrazinamide 1
5	1994	Non-controlled trial	ELAD	No	C3A cells	200 g	11	FHF 10 PNF 1	38.5 ± 18.1	5M:6F	Idiopathic 1; Virus 3; AO 2; INH 1; FIAU 3; Anhepatic 1
6	2002	Non-controlled trial	ELAD	No	C3A cells	300-400g	5	FHF 5	22.2 ± 9.4	2M:3F	asparaginase toxicity 1; Indeterminate 3; Autoimmune 1
7	2002	Phase I trial	AMC-BAL	No	Porcine hepatocytes	11.9 × 109	7	FHF 7	34.3 ± 15.2	2M:5F	Virus 4; AFLP 1; Indeterminate 2
8	2003	Case report	AMC-BAL	No	Porcine hepatocytes	10 × 109	1	FHF	35	F	Virus 1
9	1996	Non-controlled trial	NR	No	Porcine hepatocytes	5 × 109	12	FHF 11 PNF 1	37.2 ± 15.5	6M:6F	Indeterminate 4; AO 2; Virus 3; Ischemic Failure 1; Autoimmune 1; PNF 1
10	2003	Phase I trial	MELS	Yes	Porcine hepatocytes; non-parenchymal cells	(1.8-4.4) × 1010	8	FHF 8	34.3	1M:7F	Rug-related 2; Virus 3; Indeterminate 3
11	2003	Case report	MELS	Yes	Human hepatocytes	470 g	1	PNF	26	F	Intoxication with amanita phalloides
12	2002	Case report	BLSS	No	Porcine hepatocytes	70-100 g	1	FHF	41	F	Indeterminate 1
13	2002	Non-controlled trial	RFB-BAL	No	Porcine hepatocytes	200-230 g	7	FHF 4 PNF 3	37.4 ± 18.4	5M:2F	Virus 3; PNF 3; Liver trauma 1
14	2003	Non-controlled trial	HBAL	Yes	Porcine hepatocytes	1.0 × 109	12	FHF 12	41.8 ± 13.0	9M:3F	Virus 12
15	1999	Non-controlled trial	HepatAssis	Yes	Porcine hepatocytes	5 × 109	8	FHF 8	33.4 ± 11.0	1M:7F	AO 8
161	2018	Phase 1/2a Trial	LifeLiver BAL	NR	Porcine hepatocytes spheroids	NR	8	FHF 8	NR	NR	NR
17	1996	Pilot-Controlled Trial	ELAD	No	C3A cells	400 g	Group-1 17	FHF 17	30	6M:3F vs 3M:5F2	AO 5, Virus 3, ATB 5 vs AO 6, Virus 12; ATB 1
							Group-2 7	FHF 7		0M:3F vs 3M:1F2	AO 3 vs AO 3, Virus 12
18	2004	RCT	HepatAssist	Yes	Porcine hepatocytes	7 × 109	171	FHF 147 PNF 24	37	26M:60F vs 25M:60F2	Known causes 83, Indeterminate 64

¹Data from abstract;

²Intervention vs control; NA: Not applicable; NR: Not reported; Sex: Male (M) and Female (F); ELAD: Extracorporeal liver assist device; BAL: Bioartificial liver; AMC-BAL: Academic medical center bioartificial liver ; MELS: Modular extracorporeal liver support; BLSS: Novel bioartificial liver support system; RFB-BAL: Radial-flow bioreactor bioartificial liver; HBAL: Hybrid bioartificial liver; FBBAL: Fluidized bed bioartificial liver; HBALSS: Hybrid bioartificial liver support system; PNF: Primary nonfunction; FHF: Fulminant hepatic failure; AO: Acetaminophen; INH: Isoniazid; FIAU: Fialuridine; AFLP: Acute fatty liver of pregnancy; ATB: Anti-tuberculous hepatotoxicity; PERV: Porcine endogenous retrovirus; RCT: Randomized controlled trial.

Characteristics of the BAL, subjects, outcomes, and adverse events in the clinical trials

From the 18 clinical trials, 332 patients with ALF were included, with 295 cases of FHF subtypes and 37 cases of PNF subtypes. The mean age was 35.4 years, and females accounted for 69.4% of the patients according to the reported data. Most of the disease etiologies were indeterminate (103 cases), viruses (45 cases), and AO (33 cases). The types of BAL included HepatAssist (6 cases), ELAD (3 cases), AMC-BAL (2 cases), MELS (2 cases), BLSS (1 case), RFB-BAL (1 case), HBAL (1 case), Lifeliver (1 case), and BAL (1 case), and in one case the BAL type was unclear; of these 9 were hybrids and 8 were non-hybrids. Most of the cells were sourced from porcine hepatocytes (14/18), followed by C3A cells (3/18) and primary human hepatocytes (1/18). The mean cell mass was approximately 9 × 10⁹ (Table 1).

The mean treatment time was around 25 h. Among the 317 reported patients, 201 received orthotopic liver transplant (OLT) and 57 recovered without OLT. The mean survival rate in the OLT group was 93%, with the follow-up period ranging from 7 days to 62 months. Hemodynamics were stable in all patients. These results show that BAL improved liver and renal functions in all the patients, except 3 with PNF[6,14,15], in terms of the different biochemical parameters, with decreased ammonia, bilirubin, and transaminase levels in 12, 12, and 10 studies, respectively. Other meaningful indicators were reduced, including lactate ALB, BUN, and creatinine levels. By examining prothrombin time (PT), international normalized ratio, or other parameters, 9 studies found improvements in hematological and coagulative status. Ten of 12 reported studies showed an improvement in encephalopathy index. Thirteen of 16 reported studies showed improvements in neurological indicators, showing decreased intracranial pressure (ICP) and increased cerebral perfusion pressure, Glasgow coma score, and comprehensive level of consciousness score. In 3 studies on ALF subtypes, the encephalopathy index and neurological indicators showed improvements in patients with FHF but not in patients with PNF[6,14,15]. However, one case report of a patient with PNF showed improvement in the neurological status with a change in coma stage from IV to I after BAL treatment[22] (Table 2).

Table 2 Outcomes and adverse events after treating by bioartificial liver support system in clinical trials.

ID	Treating time	Bridgingtime	OLT /total		SR of OLT	SR of no OLT	Recovery without OLT	Follow-up time	Hemodynamics	Liver and renal function	Hematologic and coagulation	Encephalopathy index	Neurologic	Adverse events	PERV test
1	1.6 × 6 h	24 h	7/7		100%	NA	NA	NR	Stable	Decreased: ammonia; transaminases	Decreased: Fibrinogen	Improved	Decreased: ICP Increased: CPP	None	NR
2	2.1 × 6 h	45.3 h	16/18		100%	50%	1	NR	Stable	Decreased: ammonia; ALB; transaminases; bilirubin; BUN; creatinine Increased: glucose	Not improved	Improved	Decreased: ICP; Increased: CPP; GCS; CLOCS	Transient hypotension	NR
	1.6 × 6 h	83.0 h	3/3		100%	NA	NA	NR	Stable	Decreased: transaminases; bilirubin; ALB Increased: glucose	Not improved	Not improved	Not improved
3	1.8 × 6 h	38.6 h	14/15		100%	100%	1	2-62 m	Stable	Decreased: ammonia; bilirubin; transaminases; ALB; BUN; creatinine; Increased: Glucose	Not improved	Improved	Decreased: ICP; Increased: CLOCS	None	Negative (5 y)
	1.7 × 6 h	21 h-8 d	3/3		100%	NA	NA	2-62 m	Stable	Not improved	Not improved	Improved	Not improved
4	1.9 × 6 h	46 h	10/10		80%	NA	NA	24.5m	Stable	Decreased: bilirubin; transaminases	Decreased: Platelets; Fibrinogen	Improved	Increased: GCS; CLOCS	Bleeding; transitory hypotension	Negative
5	52.6 h	40.8 h	4/11		100%	14%	1	10 d	Stable	Improved	NR	Improved	Improved	Transitory hypotension	NA
6	50.8 h	50.8 h	5/5		80%	NA	NA	30 d	Stable	Improved	NR	Not improved	Not improved	None	NA
7	18.9 h	NR	6/7		100%	100%	1	18 m	Stable	Decreased: bilirubin; ammonia	NR	NR	Improved	Transitory hypotension	Negative -18 m
8	35 h	35 h	1/1		100%	NA	NA	15 m	Stable	Decreased: bilirubin; ammonia; lactate	Not improved	NR	Improved	NR	Negative 12 m
9	1.7 × 6 h	39.3 h	12/12		100%	NR	NR	NR	Stable	Decreased: bilirubin; ammonia; transaminases; Increased: glucose	Not improved	Improved	Decreased: ICP; Increased: CPP; CLOCS	None	NR
10	27.3 h	NR	8/8		100%	NR	NR	3y	Stable	Decreased: bilirubin; ALB	Decreased: platelets	Improved	NA	Decreased body temperature	Negative 3 y
11	79 h	79 h	1/1		100%	NR	NR	1y	Stable	Decreased: lactate; BUN; creatinine	Improved	Improved	Improved	Decreased body temperature	NA
12	12 h	7 d	NA1	NA1		NA1	NA1	7d	Stable	Decreased: lactate; ammonia; transaminases	Improved	NR	Not improved	Hypoglycemia	NR
13	11.7 h	11.7 h	6/7		83%	0%	0	NA	Stable	Decreased: bilirubin; transaminase; ammonia; lactate; urea	Improved	NR	Improved	None	Negative 180 d
14	1.1 × 6 h	NR	NA2	NA2		NR	NR	1 m	Stable	Decreased: bilirubin; transaminase; ammonia	Improved	NR	Improved	None	NR
15	2.9 × 6 h	NR	3/8		100%	100%	5	NR	Stable	Decreased: ammonia; bilirubin; transaminases; BUN; creatinine	Improved	Improved	Decreased: ICP Increased: CLOCS	None	NR
16	NR	NR	2/6		100%	75%	3	NR	NR	Decreased: ammonia	Not improved	NR	Improved	Coagulopathy pneumonia, sepsis, and diseased progression	Negative
17	72 (3-168) h	NR	2/9 vs 2/83		50% vs 50%3	6/7 vs 5/63	6 vs 53	NR	Stable	Decreased ammonia	Improved	NR	NR	Tachypnoeic; tachycardic; pyrexial; disseminated intravascular coagulation	NA
			1/3 vs 1/43		100% vs 100%3	0% vs 0%3	0 vs 03
18	17.4 h	5 d vs 3 d	45/85 vs 49/863		89% vs 80%3	50% vs 38%3	20 vs 143	30 d	Stable	Decreased bilirubin	Not improved	NR	Not improved	None	Negative 12 m

¹Suitable liver was available for OLTx during that time.

²Simultaneous HBAL 1/7 died; nonsimultaneous HBAL 2/5 died.

³Intervention vs control. NA: Not applicable; NR: Not reported; SR: Survival rate; OLT: Orthotopic liver transplantation; ALB: Albumin; BUN: Blood urea nitroge; ICP: Intracranial pressure; CPP: Cerebral perfusion pressure; GCS: Glasgow coma score; CLOCS: Comprehensive level of consciousness score; PERV: Porcine endogenous retrovirus.

During BAL treatment, 9 studies reported adverse events such as transient hypotension, decreased body temperature, tachycardia, pyrexia, and hypoglycemia, which had no clinical significance and resolved in all. PERV test results in 8 reported studies were all negative (Table 2).

Characteristics of the BAL, animal, and outcomes in the preclinical experiments with large animals

Of 12 studies that performed preclinical experiments with pigs (8 studies, 160 animals), monkeys (2 studies, 45 animals), and canines (2 studies, 40 animals), the proportions of male and female animals were 45.3% (111/245) and 30.2% (74/245), respectively. Inducers included D-galactosamine in 7 studies (145 animals)[5,12,29-33], surgical operation in 3 studies (53 animals)[11,34,35], 85% hepatectomy in 1 study (18 animals)[36], and α-amanitin and lipopolysaccharide in 1 study (30 animals)[10] (Table 3).

Table 3 Characteristics of preclinical experiments on large animals in past 10 years.

ID	Year	Animal					BAL system					Outcomes		Test for PERV
		Species	No	Sex	Weight(kg)	Inducer	Type	Cell	Mass	Bioreactor	Treatment time	Survival	Other
19	2011	Pig	30	M	10-15	D-galactosamine	FBBAL	Alginate-chitosan encapsulated primary porcine hepatocytes	5 × 109	Choanoid fluidized bed bioreactor	6 h	Survival time: BAL 72.9 ± 4.72 h Sham BAL 54.6 ± 4.09 h Control 54.8 ± 3.98 h	Decreased: lactate; glucose	NR
20	2012	Canine	32	NR	10-15	D-galactosamine	HBAL	Co-cultured porcine hepatocytes and bone marrow mesenchymal stem cells	1x 1010	Multi-layer flat-plate bioreactor + anionic resin adsorption column	3 h	7 day survival: HBAL 7/8 BAL 5/8 NBAL 4/8 Control 3/8	Decreased: transaminases; LDH; ammonia; bilirubin; PT Increased: ALB	Negative (7 d)
21	2013	Pig	13	F	25-30	Hepaticartery ligation	NA	Alginate-encapsulated HepG2cell-spheroids	5 × 1010	Fluidised-bed bioreactor	7 h	Survival time: BAL 10.5 ± 20.7 h SBAL 8.6 ± 21.4 h	Decreased: ICP; ammonia; Increased: bilirubin; acidosis	NR
22	2014	Cynomolgus monkey	15	M	6.5-7.0	D-galactosamine	HBALSS	Human hepatic CL-1 cells grown in microgravity culture	4 × 109	Perfusion bioreactor	6 h	Survival time: 128 h BAL 5/10 Control 0/5	Decreased: bilirubin; TBA; BUN; Cr; ammonia; Fischer indices Increased: ALB	NR
23	2015	Canine	8	NR	10-13	D-galactosamine	HBAL	Co-cultured porcine hepatocytes and bone marrow mesenchymal cells	1 × 1010	Multi-layer flat-plate bioreactor + anionic resin adsorption column	6 h	1 year survival: 7/8	Decreased: transaminases; PT; bilirubin; LDH; ammonia; Increased: ALB	Negative (1 year)
24	2015	Pig	18	F	45	D-galactosamine	SRBAL	Porcine hepatocytes spheroids	200 g	Spheroid reservoir	24 h	Survival 90 h (%) ST 0/6, 0% ST + Non-cell 1/6,17% ST + SRBAL 5/6, 83%	Decreased: ammonia; ICP; brain water content	NR
25	2016	Pig	21	M	10-15	D-galactosamine	FBBAL	Alginate-chitosan encapsulated porcine hepatocytes	5 × 109	Choanoid fluidized bed bioreactor	6h	Survival time: FBBAL 70.4 ± 11.5 h Sham FBBAL 51.6 ± 7.9 h Control 49.3 ± 6.6 h	Decreased: PCs; LPCs; FAs; SM; Increased: CBAs	NR
26	2016	Pig	20	NR	15-25	D-galactosamine	HiHep-BAL	HiHeps	3 × 109	Multi-layer radial-flow bioreactor	3h	Survival 7 d: hiHep-BAL 7/8 Empty-BAL 1/6 No-BAL 0/6	Decreased: transaminase ammonia; bilirubin; PT	NR
27	2017	Pig	25	F	30-35	Surgical ligation of all blood flow to the liver	UCLBAL	3-dimensional (3D) HepG2-cell spheroids	7.3 × 1010	Fuidised bed bioreactor	6h	Survival time: Control-BAL 7.04 ± 1.9h, n = 15 Cell-BAL 8.21 ± 2.3 h, n = 13	Decreased: PT; INR; ICP; ammonia	NR
28	2017	Pig	15	M	45-55	Complete hepatic inflow devascularization	NA	Ca-alginate-immobilized hepatocyte spheroids	2 × 1010	Packed-bed bioreactor	12h	Median survival time: Control 21 h n = 5 BAL 28.5 h n = 5 Cell-free BAL 21 h n = 5	Decreased: ammonia; creatinine ICP; BP Increased: urine	NR
29	2018	Rhesus monkey	30	M	10-20	α-amanitin and lipopolysaccharide	SRBAL	Pig hepatocyte-HUVEC organoids	2.6 × 1010	Spheroid reservoir	6 h	Median survival time: SRBAL 12 h 336 h n = 6 SRBAL 24 h 248 h n = 6 SRBAL 36 h 132 h n = 6 Sham no-cell SRBAL 12 h 90 h n = 6 Control 60.5 h n = 6	Decreased: ammonia; bilirubin Increased: albumin	Negative (6 h)
30	2019	Pig	18	F	20-30	85% hepatectomy	SRBAL	Porcine hepatocyte spheroids	200g	Spheroid reservoir	24 h	Survival rate at 90 h: SMT 0/6 SMT plus no-cell SRBAL 0/6 SMT plus SRBAL (200 g) 5/6	Decreased: ammonia; ICP; INR Increased: volume regeneration	NR

NA: Not applicable; NR: Not reported; BAL: Bioartificial liver; Sex: Male (M) and Female (F); ELAD: Extracorporeal liver assist device; AMC-BAL: Academic medical center bioartificial liver; MELS: Modular extracorporeal liver support; BLSS: Novel bioartificial liver support system; RFB-BAL: Radial-flow bioreactor bioartificial liver; HBAL: Hybrid bioartificial liver; FBBAL: Fluidized bed BAL; HBALSS: Hybrid bioartificial liver support system; SRBAL: Spheroid reservoir bioartificial liver; hiHep: Human-induced hepatocytes; CBAs: Conjugated bile acids; PCs: Phosphatidylcholines; LPCs: Lysophosphatidylcholines; FAs: Fatty acids; SM: Sphingomyelin; ICP: Intracranial pressure; ALB: Albumin; PT: Prothrombin time; INR: International normalized ratio; PERV: Porcine endogenous retrovirus.

The types of BAL included SRBAL (n = 3), HBAL (n = 2), FBBAL (n = 1), UCLBAL (n = 1), hiHep-BAL (n = 1), HBALSS (n = 1), FBBAL (n = 1), and BAL (n = 1), using cells from porcine hepatocyte (9/12), human hepatic CL-1 cells or HepG2 cells (2/12), and HiHeps (1/12), which were all cultured using modified three-dimensional methods such as spheroids, organoid, alginate-chitosan encapsulated, and even microgravity culture, with corresponding bioreactors such as a spheroid reservoir. The mean cell mass was 2 × 10¹⁰, and the treatment time ranged from 3 to 24 h (mean: 9 h; Table 3).

Compared with the control group, the survival outcomes (median survival time or survival rate) were better in the BAL group, and the biochemical metabolic function showed improvement, especially decreased ammonia levels (10/12), bilirubin levels (6/12), ICP (5/12), and PT (4/12). All the PERV test results were negative in reported studies (Table 3).

Meta-analysis of the effects of the BAL on mortality in the clinical trials and preclinical experiments

As shown in Figure 2, the overall effect of the BAL on mortality in the patients with ALF[6,7] was insignificant [BAL 97 vs control 98: RR (95%CI), 0.72 (0.48-1.08)]. However, the meta-analysis of the preclinical experiments of large animals[10,12,29,30,32,36] indicated a significant effect of the BAL [BAL 56 vs control 77: RR (95%CI), 0.27 (0.12-0.62)]. The test of heterogeneity showed no significant difference between included studies, with I² being 0% and 41% for human clinical studies and pre-clinical experimental studies, respectively.

Figure 2 Effect of bioartificial liver support systems on mortality in acute liver failure humans and large animals. The randomized controlled trials for meta-analysis included 2 clinical trials and 6 preclinical experiments with death events (or survival rate) recorded between 90 h to 7d after application of bioartificial liver support systems. M-H: Mantel-Hanszel; BAL: Bioartificial Liver; CI: Confidence interval.

Sensitivity analyses of pooled results using an alternative effect measure (M-H OR = 0.61, 95%CI: 0.33-1.11 for humans; OR = 0.05, 0.01-0.17 for animals), pooling method (Peto fixed effects OR = 0.61, 95%CI: 0.34-1.11 for humans; OR = 0.07, 0.03-0.15 for animals), and statistical model (fixed effects M-H RR = 0.72, 95%CI: 0.48-1.08 for humans; RR = 0.24, 0.13-0.44 for animals) showed similar findings.

As shown in Supplemental Figure, we observed publication bias and found none in the clinical trials, and little in the preclinical experiment studies. However, it remains unclear because of the small number of included studies.

Bias risk of included RCT and non-RCT studies

By bias assessment, all the included RCT studies were regarded as low or middle-risk overall, with 4 to 6 of 7 items listed by the Cochrane assessment standards for RCT assessed as low risk (Supplemental Table 2). For non-RCT studies, all the clinical trials among humans scored 5 or 6 (total score: 9), indicating a low or middle risk, while those of pre-clinical experiments scored a little higher, with most scoring 7 or 8 (Supplemental Table 3).

DISCUSSION

Main findings and interpretations

By conducting a systematic review of 18 clinical trials and 12 preclinical experiment in large animals, including a meta-analysis of selected studies, we suggest that the BAL might reduce mortality from ALF in large animals, but not in humans [BAL vs control: RR (95%CI), 0.27 (0.12-0.62) for animals and 0.72 (0.48-1.08) for humans], with no heterogeneity observed between included studies. Compared with the preclinical experiments, most of the clinical trials were conducted more than 10 years ago. Moreover, the BAL used in large animals has undergone an obvious improvement regarding the type, cell source, cell mass, and bioreactor. All the studies showed improvements in liver and renal functions, hematologic and coagulative parameters, encephalopathy index, and neurological indicators after the treatment with BAL, with neither significant adverse events nor PERV infection.

At present, whether the BAL is able to reduce mortality in the ALF population remains controversial. For example, a meta-analysis performed in 2011[8] indicated that BAL appeared to affect mortality in patients with ALF, while another three meta-analyses of clinical controlled trials conducted by Liu et al[37], Kjaergard et al[3], and Zheng et al[38] demonstrated that the use of the BAL was not associated with the improvement of survival outcome among patients with ALF, which is consistent with our study.

The quality of the BAL is the most important indicator that affects the outcome and adverse events of BAL treatment for ALF, which might support the effect difference between clinical trials and preclinical experiments. As reported in our study, cell source, culture mode, cell mass, and the bioreactor of the BAL were different between the two types of study.

There are currently four main sources of cells for the BAL and their pros and cons are as follows: (1) Human primary hepatocytes are the most suitable cells but are limited by low availability due to a shortage of donor organs[38]; (2) Immortalized human hepatoblastoma cell lines (HepG2/C3A/hepatic CL-1) are sufficiently expanded but are considered to have less metabolic functions than primary hepatocytes[39]; (3) Human-induced hepatocytes (hiHep) were reported to have a potential for metabolic detoxification[12], but it is difficult to meet the demands on a clinical scale because of the cost and complexity of hiHep; and (4) Porcine hepatocytes are the main cells used in the BAL and have similar function with human hepatocytes, are readily available, and are low-cost. Although no PERV infection has been found in 42 patients with long-term immunosuppression and 13 healthcare workers after a follow-up of 5-8 years by a new highly sensitive and specific quantitative real-time polymerase chain reaction assay[40,41], xenozoonosis and the potential risks of PERV infection after treatment remain a concern.

In addition, primary hepatocytes easily lose their function in vitro during long-term monolayer culture[42]. In the preclinical experiments, to maintain and improve the viability and metabolic functions of hepatocytes, cells were cultured in a three-dimensional environment to simulate microgravity to form spheroids[30,32,36] or organoids[10], and alginate-chitosan encapsulated spheroids[5,11,33]. Hepatocytes were also co-cultured with bone marrow mesenchymal cells and human umbilical vein endothelial cells to maintain the function of porcine hepatocytes by providing cell-to-cell interactions[10,29,31,43]. In addition, to adapt to the changes of the cells, bioreactors were modified as spheroid reservoirs and multi-layer radial-flow bioreactors to provide a suitable environment for hepatocytes to survive and maintain their cell functions.

Adequate liver cell mass is another crucial indicator for evaluating the BAL, and the innovation requires a higher number of hepatocytes and enhanced function during long-term culture[44]. It has been widely suggested that approximately 30% of the total liver volume is required for survival and that 10-40 billion liver cells without loss of function would be required for BAL treatment[45,46]. Therefore, the low functionality and availability of cells for the clinical scale mass of all the BAL might explain the insignificant effect based on the meta-analysis of the two controlled clinical trials in comparison with the preclinical experiments.

Furthermore, in the preclinical experiments, the subjects in each study were the homogeneous ALF models, but in the clinical trials, the etiologies of ALF varied and were complex, which might have led to different effects of the BAL. In comparison to the patients with PNF, the patients with FHF showed a strikingly different effect of the BAL treatment in a randomized multicenter controlled trial[6] and two non-controlled clinical trials[14,15]. Only unremarkable metabolic effects were observed in the patients with PNF, without amelioration of the neurological state and survival benefit after BAL treatment, whereas an improvement in neurological state and benefit were observed in the patients with FHF, even though one case report on PNF showed a great improvement in neurological state with a change in coma stage from IV to I after treatment with MELS[22].

Strengths and limitations

Our study has several strengths. First, by using a systematic searching strategy and selection procedures, we included all the clinical trials of BAL for ALF and preclinical experiments on large animals in the recent decade, which might represent a current overview of research in this domain, making our study probably the first review to provide evidence for future research. Second, we calculated the combined effect of BAL for ALF by performing a meta-analysis of RCT studies stratified according to clinical trial and preclinical experiment, making the effects comparable between the two study types; meanwhile, the bias of all the included studies was assessed as low to middle-risk and the publication bias was subtle. Finally, we created a detailed checklist of all the potential information associated with the outcome of BAL. Two independent reviewers conducted data extraction, ensuring quality data and allowing for examination of the gap between preclinical experiments and clinical trials.

Our study has two main limitations. One is that the number of RCT clinical trials included was limited to meta-analyses even if many studies have been conducted on ALF and other liver diseases such as acute-on-chronic liver failure. Nevertheless, our data could be usable. Thus, the overall effect of BAL for ALF in humans was desirable but must be verified in the future. Another limitation is that it was not necessary or proper for us to use a meta-regression for controlling covariates, because there existed no heterogeneity between included studies and the limited number of included studies did not meet the requirement of the precondition for regression. Thus, we could not provide further evidence for future research and practice.

Suggestions for future research

Based on the results of our study, we suggest the following for future clinical trials, preclinical experiments, and transformations. First, alternative cells or methods for acquiring high-quality liver cells in vitro must be identified to achieve clinical-scale goals. Second, the effects of the subgroups, patients with PNF or FHF, and patients with different etiologies should be determined and examined in clinical trials in the future. Finally, the advanced BAL, which proved to have a significant benefit on the survival outcome of the large-animal ALF model, should undergo clinical transformation as much as possible.

ARTICLE HIGHLIGHTS

Research background

Acute liver failure (ALF) has a high mortality varying from 80% to 85% with rapid progress in multi-organ system failure. Bioartificial liver (BAL) support systems have a potential effect to provide temporary support to bridge patients with acute liver failure to liver transplantation or spontaneous recovery. In the past decades, several BAL support systems have been conducted in clinical trials, but remained verified. More recently, concerns have been raised on the renovation of high-quality cell sources and configuration of BAL support systems to provide more benefits to ALF models in preclinical experiments.

Research motivation

A systematic review and meta-analysis of the existing literature on the use of BAL among humans and large animals with ALF could help bridge the gap between preclinical experiments and clinical trials regarding the effect of BAL for treating acute liver failure.

Research objectives

To investigate the characteristics of studies about BAL for ALF, and to evaluate their effects on mortality.

Research methods

Eligible clinical trials and preclinical experiments on large animals were identified on Cochrane Library, PubMed, and EMbase up to March 6, 2019. Two reviewers independently extracted the necessary information, including the key BAL indicators, survival and indicating outcomes, and adverse events during treatment. Descriptive analysis was used to identify the characteristics of the included studies, and a meta-analysis by including only RCT studies was performed to combine the overall effect of BAL on mortality among humans and large animal, respectively.

Research results

Of 30 selected studies, 18 were clinical trials and 12 were preclinical experiments. The meta-analysis results suggested that BAL might reduce the mortality of ALF in large animals, probably due to the recent improvement of BAL, including the type, cell source, cell mass, and bioreactor, but seemed ineffective for humans. Liver and renal functions, hematologic and coagulative parameters, encephalopathy index, and neurological indicators seemed to improve after BAL, with neither meaningful adverse events nor porcine endogenous retrovirus infection.

Research conclusions

BAL may reduce the mortality of ALF by bridging the gap between preclinical experiments and clinical trials. Clinical trials using improved BAL must be designed scientifically and conducted in the future to provide evidence for transformation.

Research perspectives

Our study could provide some suggestions for future clinical trials, preclinical experiments, and transformations. First, alternative cells or methods for acquiring high-quality liver cells in vitro must be identified to achieve clinical-scale goals. Second, the effects of the subgroups, patients with PNF or FHF, and patients with different etiologies should be determined and examined in clinical trials in the future. Finally, the advanced BAL, which proved to have a significant benefit on the survival outcome of the large-animal ALF model, should undergo clinical transformation as much as possible.