# Adalimumab Therapy for Crohn's Disease and Axial Spondyloarthritis in Latent Tuberculosis: A bibliometric-systematic literature review

**Authors:** Nyimas Maida Shofa, Nurike Setiyari Mudjari, Rusdiyana Ekawati, Arianti Arianti, Annisa Zahra Mufida, Budi Widodo, Titong Sugihartono

PMC · DOI: 10.18295/2075-0528.2971 · Sultan Qaboos University Medical Journal · 2026-02-21

## TL;DR

This paper reviews the use of adalimumab for Crohn's disease and arthritis in areas with high tuberculosis risk, finding it effective but with some risk of TB reactivation.

## Contribution

The study provides a bibliometric and systematic review of adalimumab's use in TB-endemic regions with concurrent TB prophylaxis.

## Key findings

- Adalimumab achieved 60–85% clinical remission in moderate-to-severe Crohn's disease and axial spondyloarthritis.
- 1–3% of patients developed active TB despite screening and isoniazid prophylaxis.
- Region-specific frameworks are needed for safe adalimumab use in TB-endemic areas.

## Abstract

The management of Crohn's disease (CD) using anti-tumour necrosis factor therapy in tuberculosis (TB)-endemic regions poses major clinical challenges due to the risk of latent TB infection reactivation. This bibliometric–systematic literature review synthesised evidence from 17 peer-reviewed studies (2020–2025) evaluating adalimumab administered with concurrent prophylactic antitubercular therapy. Thematic synthesis and bibliometric mapping using VOSviewer demonstrated that adalimumab achieved 60–85% clinical remission in moderate-to-severe CD and axial spondyloarthritis while enhancing mucosal healing. However, 1–3% of patients developed active TB despite appropriate screening and isoniazid prophylaxis, revealing false-negative diagnostics and partial chemoprophylaxis protection. These findings highlight the need for region-specific frameworks integrating multimodal screening, targeted prophylaxis and ongoing clinical surveillance. Adalimumab remains a cornerstone biologic in TB-endemic settings, but its safe use requires adaptive, context-driven protocols emphasising vigilant risk mitigation.

## Linked entities

- **Chemicals:** isoniazid (PubChem CID 3767)
- **Diseases:** Crohn's disease (MONDO:0005011), tuberculosis (MONDO:0018076)

## Full-text entities

- **Genes:** IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** latent TB (MESH:D055985), AxSpA (MESH:D000089183), CD (MESH:D003424), infection (MESH:D007239), venous thromboembolism (MESH:D054556), RA (MESH:D001172), EIM (OMIM:605021), infectious (MESH:D003141), ulcerative colitis (MESH:D003093), herpes zoster (MESH:D006562), TB (MESH:D014376), granulomas (MESH:D006099), IBD (MESH:D015212), B (MESH:D006509), tumour necrosis factor (MESH:D009369), inflammation (MESH:D007249), latent (MESH:D000085343), ankylosing spondylitis (MESH:D013167), immune-mediated inflammatory diseases (MESH:C567355)
- **Chemicals:** vedolizumab (MESH:C543529), mirikizumab (MESH:C000708407), tofacitinib (MESH:C479163), azathioprine (MESH:D001379), upadacitinib (MESH:C000613732), thiopurines (MESH:C520399), INH (MESH:D007538), ustekinumab (MESH:D000069549), risankizumab (MESH:C000601773), infliximab (MESH:D000069285), Adalimumab (MESH:D000068879)
- **Species:** Homo sapiens (human, species) [taxon 9606], Meleagris gallopavo (common turkey, species) [taxon 9103]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12969460/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12969460/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969460/full.md

---
Source: https://tomesphere.com/paper/PMC12969460