CXCR3 is associated with T-cell-induced heart damage in acute rheumatic fever

T cells. However, elevation of the chemokine CCL5 and immunoglobulin IgG3, along with reduced expression of the chemokine receptor CXCR3 in the T cell compartment distinguished ARF from all other groups. Immunofluorescence imaging of rheumatic valve tissue confirmed a role for CXCR3-mediated T cell tissue homing during inflammatory disease. Together with a reduced frequency of circulating regulatory T cells, these data underscore a perturbed T cell compartment and provide a rationale for exploring currently available immune-modulating therapies to treat ARF.

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Publication Details

Journal
Nature Communications
Published
2026-03-31
DOI
https://doi.org/10.1038/s41467-026-71094-8
Primary Topic
Streptococcal Infections and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

CXCR3 is associated with T-cell-induced heart damage in acute rheumatic fever

David Broadhurst, Florina Chan Mow, Mark Mayo, Glenn Pearson et al.
Nature Communications
Streptococcal Infections and Treatments
article

CXCR3 is associated with T-cell-induced heart damage in acute rheumatic fever

David Broadhurst, Florina Chan Mow, Mark Mayo, Glenn Pearson, Nigel Wilson, Saem Mul Park, Michael Serralha, Nicole J. Moreland, Anna P. Ralph, Anna E. S. Brooks, Timothy C. Barnett, Ciara Ramiah, Natalie Lorenz, Reuben McGregor, F. M. Middleton, Johann Brink, Judith Tresidder, Julie Bennett, Sarah Kilian, William Jeffery Martin, Jonathan Carapetis, P. Rod Dunbar
article en

Abstract

T cells. However, elevation of the chemokine CCL5 and immunoglobulin IgG3, along with reduced expression of the chemokine receptor CXCR3 in the T cell compartment distinguished ARF from all other groups. Immunofluorescence imaging of rheumatic valve tissue confirmed a role for CXCR3-mediated T cell tissue homing during inflammatory disease. Together with a reduced frequency of circulating regulatory T cells, these data underscore a perturbed T cell compartment and provide a rationale for exploring currently available immune-modulating therapies to treat ARF.

Nature Communications
Edith Cowan University (AU), University of Auckland (NZ), The Kids Research Institute Australia (AU), The University of Western Australia (AU), Princess Margaret Hospital for Children (AU), Charles Darwin University (AU), Menzies School of Health Research (AU), Maurice Wilkins Centre (NZ), Royal Darwin Hospital (AU), Starship Children's Health (NZ), Perth Children's Hospital, University of Otago (NZ)
Stan Perron Charitable Foundation, Medical Research Council, National Health and Medical Research Council, Health Research Council of New Zealand
Good health and well-being
Openalex Percentile: Top 28%
Streptococcal Infections and Treatments
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