Evidence map›Paper›PMID 41291898›Full record

ArticleJournal of medical case reports2025

Management of refractory autoimmune hepatitis with rituximab: a case series.

Nicholas M Batt, Stephen D Bloom, Geoffrey Haar, Amanda J Nicoll

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Nicholas M BattDepartment of Gastroenterology, Austin Health, Heidelberg, Melbourne, VIC, Australia. Nicholas.batt2@austin.org.au.ORCID http://orcid.org/0000-0002-0845-3341
Stephen D BloomDepartment of Gastroenterology, Eastern Health, Box Hill, Melbourne, VIC, Australia.
Geoffrey HaarDepartment of Gastroenterology, Eastern Health, Box Hill, Melbourne, VIC, Australia.
Amanda J NicollDepartment of Gastroenterology, Eastern Health, Box Hill, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsMost patients with autoimmune hepatitis respond to the standard of care of prednisolone in combination with a thiopurine, or a second line of mycophenolate mofetil or tacrolimus. This study aims to add to the reported experience of using rituximab in the small numbers of patients with autoimmune hepatitis who are refractory or intolerant to these treatments. CASE PRESENTATION: A retrospective single center case series was performed on six patients who were treated with rituximab for probable or definite, biopsy-proven type 1 autoimmune hepatitis over a 9-year period. They were Caucasian, three males and three females, with an age at autoimmune hepatitis diagnosis ranging from 16 to 52 years old. Three patients had cirrhosis. All six patients had trialed prednisolone, a thiopurine, and also mycophenolate mofetil prior to the rituximab. Indications for rituximab were treatment of an autoimmune hepatitis flare and potential intolerance to the second line therapy. For patients with autoimmune hepatitis flare, rituximab improved transaminases and/or total immunoglobulin G levels, lowered prednisolone dosage, and reduced the number or dose of disease-modifying agents. Four of the six cases required more than one dose of rituximab. Dosage intervals ranged from 1 month to 5 years. In one case, rituximab also effectively treated comorbid immune thrombocytopenia. No complications arose from rituximab treatment.

conclusionRituximab appears safe, and also effective in some patients with autoimmune hepatitis who have been refractory to standard of care. The dose reduction for other disease modifying agents makes rituximab an attractive option for this difficult to treat subset of patients.

Indexed as

Hepatitis, AutoimmuneImmunologic FactorsImmunosuppressive AgentsRituximabAdolescentAdultFemaleHumansMaleMiddle AgedPrednisoloneRetrospective StudiesTreatment OutcomeYoung AdultImmunologic FactorsImmunosuppressive AgentsPrednisoloneRituximabAnti-CD20Autoimmune hepatitisCase reportRefractoryRituximab

Identifiers

PMID41291898
PMCPMC12645696

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.