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TNF inhibitor therapy is associated with an increase in absolute lymphocyte count that is, in turn, associated with lower mortality across the spectrum of immune-mediated inflammatory diseases
Frontiers in Immunology

Cure8 research brief

TNF inhibitor therapy is associated with an increase in absolute lymphocyte count that is, in turn, associated with lower mortality across the spectrum of immune-mediated inflammatory diseases

2 min read
Research and clinical trials Anti-TNF Biomarkers Clinical study Adult patients Clinicians Researchers Patients On Biologics

Why This Matters

An increase in absolute lymphocyte count after starting TNF inhibitors was associated with lower mortality across several immune-mediated diseases; patients and clinicians may find this biomarker and its link to outcomes of interest when discussing treatment effects and monitoring.

Who Should Pay Attention

Adult patients with IBD or other immune-mediated inflammatory diseases, clinicians who prescribe biologic or targeted therapies, researchers studying biomarkers or drug effects, and patients currently on or considering TNF inhibitors.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

The researchers used a large Veterans Affairs electronic health-record cohort to compare ALC changes after starting different biologic and targeted synthetic DMARD classes (including TNF inhibitors, JAK inhibitors, IL-12/23 and IL-23 inhibitors, IL-17 and IL-6 inhibitors, and abatacept).

TNF inhibitors were linked with a modest average increase in ALC that was larger than the changes seen with other drug classes. The analysis found that greater baseline ALC and an increase in ALC after treatment were both associated with improved survival, after adjusting for demographics and comorbidity.

The authors state it remains unclear whether the ALC increase is a causal mechanism improving longevity or instead a prognostic biomarker.

Keep In Mind

The report is based on VA electronic health-record data and is observational; associations do not prove causation. The abstract-level summary was used to prepare this note.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Research paper Evidence type derived from source or registry metadata.
PublicationFrontiers in Immunology
PublisherFrontiers Media SA
AuthorsLenche Kostadinova, Brigid Wilson, Hinnah Siddiqui +8 more
Study typeJournal Article
Indexed viaCrossref
Source typeResearch paper
PublishedNov 10, 2026, 12:00 AM
Content availableJournal abstract

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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