Evidence map›Paper›PMID 42221365›Full record

ArticleOpen forum infectious diseases2026

Antibody-Dependent Immune Complex Signaling and Inflammatory Cytokine Responses in Acute Febrile Illness: A Mechanistic Study in Arboviral and Leptospiral Infection.

Peter Mac Asaga, Vijeesh Kadukkatti, Philomena Airiohuodion, Brijil Mathew, Sunday Omilabu

Abstract read
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Article in Open forum infectious diseases, 2026. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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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

5 authors.

Peter Mac AsagaInstitute for Infection Prevention and Control, Medical Center, University of Freiburg, Breisacher str 115b, 79106 Freiburg, Germany.ORCID https://orcid.org/0000-0003-0038-8896
Vijeesh KadukkattiRWTH Uniklinik, Aachen, Institute of Occupational Health, Social and Enviromental Medicine, Pauwelsstr 30, 52074 Aachen, Germany.
Philomena AiriohuodionSpecial Programme for Research and Training in Tropical Diseases, World Health Organization, Geneva, Switzerland.
Brijil MathewAster MIMS Hospital, Kannur 670621, Kerala, India.
Sunday OmilabuCHAHZY Central Research Laboratory, College of Medicine, University of Lagos, Lagos, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Arboviral infections are characterized by heterogeneity in inflammatory responses and clinical outcomes. While antibodies are essential for protection, antibody-antigen immune complexes may modulate innate immune signaling through Fc receptor engagement. The extent to which immune complex signaling contributes to coordinated cytokine responses in human arboviral infection remains incompletely defined. Methods: We conducted a mechanistic immunology study nested within a prospective cohort of patients with acute arboviral infection in southern India. Using paired ex vivo stimulation assays, we compared cytokine responses following antigen-only and antibody-antigen immune complex stimulation. Fc dependence was interrogated using Fcγ receptor blockade and immunoglobulin G (IgG) subclass depletion. Cytokines were quantified using the LEGENDplex Human Inflammation Panel (BioLegend). Principal component analysis was applied to identify coordinated cytokine response patterns, and multivariable regression models were used to assess associations with humoral immune state. Results: Among 80 participants, immune complex stimulation was associated with higher concentrations of pro-inflammatory cytokines compared with antigen alone. This difference was attenuated by Fcγ receptor blockade and was influenced by antibody subclass composition. Principal component analysis revealed a coordinated cytokine pattern characterized by positive contributions from interleukin-6 (IL-6), tumor necrosis factor, IL-1β, and CXCL10, with an inverse contribution from IL-10. In multivariable analysis, individuals with lower neutralization capacity or altered IgG subclass profiles exhibited higher inflammatory cytokine program scores ( Conclusions: These findings suggest that antibody-dependent immune complex signaling may contribute to inflammatory cytokine responses during acute arboviral and leptospiral infection.

Indexed as

antibody-dependent enhancementarboviruscytokineFc receptorimmune complex

Identifiers

PMID42221365
PMCPMC13218447

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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.