Talamini, Laura, Fonseca, Dennyson Leandro M, Kanduc, Darja et al. · Frontiers in immunology · 2025 · DOI
This study looked at whether COVID-19 infection, especially long COVID, might trigger the body's immune system to attack its own reproductive cells through a process called molecular mimicry—where the virus shares similar protein patterns with cells involved in sperm production. Researchers found that people with long COVID, particularly women, developed antibodies (immune proteins) that reacted with viral proteins in ways that could potentially affect fertility. The findings suggest that some long COVID patients may develop autoimmune responses that target reproductive tissues, though more research is needed to understand if this actually causes fertility problems.
For ME/CFS and long COVID patients, this research is important because it identifies a potential mechanism by which post-viral autoimmune responses could affect reproductive health—a significant quality-of-life concern. Understanding these autoimmune mechanisms may help explain systemic complications in long COVID and inform future diagnostic and therapeutic approaches for post-viral conditions affecting multiple organ systems.
This study does not establish that COVID-19 or long COVID actually causes infertility in humans—it identifies autoantibodies and their potential to interact with testicular tissue in laboratory conditions. The presence of cross-reactive antibodies does not necessarily mean they cause clinical disease; further human studies with fertility outcome measures are required. Additionally, the findings are primarily from in vitro and animal model experiments, which may not fully translate to human pathophysiology.
About the PEM badge: “PEM required” means post-exertional malaise was an explicit required diagnostic criterion for participant inclusion in this study — not that PEM was studied, observed, or discussed. Studies using criteria that do not require PEM (e.g. Fukuda, Oxford) are tagged “PEM not required”. How the atlas works →
The first block is for the primary paper and is the citation you should use in research work. The atlas-snapshot line only applies if you are specifically referring to this atlas’s reading of the paper on the date shown.
Primary citation
Talamini, Laura, Fonseca, Dennyson Leandro M, Kanduc, Darja, Chaloin, Olivier, Verdot, Cindy, Galmiche, Christian, et al. (2025). Long COVID-19 autoantibodies and their potential effect on fertility.. Frontiers in immunology. https://doi.org/10.3389/fimmu.2025.1540341
BibTeX
@article{mecfsatlas-talamini-2025-long-covid,
author = {Talamini, Laura and Fonseca, Dennyson Leandro M and Kanduc, Darja and Chaloin, Olivier and Verdot, Cindy and Galmiche, Christian and Dotan, Arad and Filgueiras, Igor Salerno and Borghi, Maria Orietta and Meroni, Pier Luigi and Gavrilova, Natalia Y and Ryabkova, Varvara A and Churilov, Leonid P and Halpert, Gilad and Lensch, Christian and Thurner, Lorenz and Fong, Siew-Wai and Ng, Lisa F P and Rénia, Laurent and Young, Barnaby E and Lye, David Chien and Lozano, José Manuel and Cabral-Marques, Otávio and Shoenfeld, Yehuda and Muller, Sylviane},
title = {Long COVID-19 autoantibodies and their potential effect on fertility.},
journal = {Frontiers in immunology},
year = {2025},
doi = {10.3389/fimmu.2025.1540341},
note = {PubMed: 40496870},
url = {https://www.mecfsatlas.com/evidence/talamini-2025-long-covid},
}Atlas snapshot reference
ME/CFS Atlas. Generator v1 / Scanner v1.4 / policy v0.1. Accessed 2026-05-29. https://www.mecfsatlas.com/evidence/talamini-2025-long-covid
Contribute
Private, reviewed by a human. Not a public comment thread.