» Articles » PMID: 32314694

Liver Enzyme Elevations in Volunteer Infection Studies: Findings and Recommendations

Overview
Specialty Tropical Medicine
Date 2020 Apr 22
PMID 32314694
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Malaria volunteer infection studies (VISs) accelerate new drug and vaccine development. In the induced blood-stage malaria (IBSM) model, volunteers are inoculated with erythrocytes infected with . Observations of elevated liver enzymes in the IBSM model with new chemical entities (NCEs) promoted an analysis of available data. Data were reviewed from eight IBSM studies of seven different NCEs, plus two studies with the registered antimalarial piperaquine conducted between June 2013 and January 2017 at QIMR Berghofer, Brisbane, Australia. Alanine aminotransferase (ALT) was elevated (> 2.5 times the upper limit of normal [×ULN]) in 20/114 (17.5%) participants. Of these, 8.9% (10/114) had moderate increases (> 2.5-5 × ULN), noted in seven studies of six different NCEs ± piperaquine or piperaquine alone, and 8.9% (10/114) had severe elevations (> 5 × ULN), occurring in six studies of six different NCEs ± piperaquine. Aspartate aminotransferase (AST) was elevated (> 2.5 × ULN) in 11.4% (13/114) of participants, across six of the 10 studies. Bilirubin was > 2 × ULN in one participant. Published data from other VIS models, using sporozoite inoculation by systemic administration or mosquito feeding, also showed moderate/severe liver enzyme elevations. In conclusion, liver enzyme elevations in IBSM studies are most likely multifactorial and could be caused by the model conditions, that is, malaria infection/parasite density and/or effective parasite clearance, or by participant-specific risk factors, acetaminophen administration, or direct hepatotoxicity of the test drug. We make recommendations that may mitigate the risk of liver enzyme elevations in future VISs and propose measures to assist their interpretation, should they occur.

Citing Articles

Longitudinal changes in iron homeostasis in human experimental and clinical malaria.

Woolley S, Grigg M, Marquart L, Gower J, Piera K, Nair A medRxiv. 2024; .

PMID: 38196596 PMC: 10775340. DOI: 10.1101/2023.12.19.23300265.


Safety, Tolerability, and Parasite Clearance Kinetics in Controlled Human Malaria Infection after Direct Venous Inoculation of Plasmodium falciparum Sporozoites: A Model for Evaluating New Blood-Stage Antimalarial Drugs.

Chughlay M, Chalon S, El Gaaloul M, Gobeau N, Mohrle J, Berghmans P Am J Trop Med Hyg. 2022; 107(4):804-814.

PMID: 36037868 PMC: 9651526. DOI: 10.4269/ajtmh.21-1297.


Hepatic safety and tolerability of cipargamin (KAE609), in adult patients with Plasmodium falciparum malaria: a randomized, phase II, controlled, dose-escalation trial in sub-Saharan Africa.

Ndayisaba G, Yeka A, Asante K, Grobusch M, Karita E, Mugerwa H Malar J. 2021; 20(1):478.

PMID: 34930267 PMC: 8686384. DOI: 10.1186/s12936-021-04009-1.


Posttreatment Transaminase Elevations in Controlled Human Malaria Infection and Naturally Acquired Malaria.

Odedra A, Woodford J, Chalon S, Barber B, McCarthy J J Infect Dis. 2021; 225(5):926-927.

PMID: 34610127 PMC: 8889285. DOI: 10.1093/infdis/jiab502.


A Longitudinal Cohort Study Using a Modified Child-Pugh Score to Escalate Respiratory Support in COVID-19 Patients - Hubei Province, China, 2020.

Xiong Y, Ma Y, Tian Y, Zhang C, Yang W, Liu B China CDC Wkly. 2021; 3(20):423-429.

PMID: 34594905 PMC: 8392970. DOI: 10.46234/ccdcw2021.113.


References
1.
Douros A, Bronder E, Klimpel A, Erley C, Garbe E, Kreutz R . Drug-induced kidney injury: A large case series from the Berlin Case-Control Surveillance Study
. Clin Nephrol. 2017; 89 (2018)(1):18-26. DOI: 10.5414/CN109212. View

2.
Shapiro T, Ranasinha C, Kumar N, Barditch-Crovo P . Prophylactic activity of atovaquone against Plasmodium falciparum in humans. Am J Trop Med Hyg. 1999; 60(5):831-6. DOI: 10.4269/ajtmh.1999.60.831. View

3.
Obiero J, Shekalaghe S, Hermsen C, Mpina M, Bijker E, Roestenberg M . Impact of malaria preexposure on antiparasite cellular and humoral immune responses after controlled human malaria infection. Infect Immun. 2015; 83(5):2185-96. PMC: 4399069. DOI: 10.1128/IAI.03069-14. View

4.
de Mast Q, van Dongen-Lases E, Swinkels D, Nieman A, Roestenberg M, Druilhe P . Mild increases in serum hepcidin and interleukin-6 concentrations impair iron incorporation in haemoglobin during an experimental human malaria infection. Br J Haematol. 2009; 145(5):657-64. DOI: 10.1111/j.1365-2141.2009.07664.x. View

5.
Krishna S, Pukrittayakamee S, Supanaranond W, Ter Kuile F, Ruprah M, Sura T . Fever in uncomplicated Plasmodium falciparum malaria: randomized double-'blind' comparison of ibuprofen and paracetamol treatment. Trans R Soc Trop Med Hyg. 1995; 89(5):507-9. DOI: 10.1016/0035-9203(95)90087-x. View