Soluble CD52 mediates immune suppression by human seminal fluid

Seminal fluid provides for the carriage and nutrition of sperm, but also modulates immunity to prevent allo-rejection of sperm by the female. Immune suppression by seminal fluid has been associated with extracellular vesicles, originally termed prostasomes, which contain CD52, a glycosylated glycophosphoinositol-anchored peptide released from testicular epithelial cells. Previously, we reported that human T cell-derived CD52, bound to the danger-associated molecular pattern protein, high mobility group box 1 (HMGB1), suppresses T cell function via the inhibitory sialic acid-binding immunoglobulin-like lectin-10 (Siglec-10) receptor. Here we show that human seminal fluid contains high concentrations of CD52 complexed with HMGB1, which mediates T cell suppression indirectly via Siglec-7 on antigen-presenting cells. Proliferation of natural killer (NK) cells, which express Siglec-7 and play a key role in the immune defence of the uterus, was directly suppressed by seminal fluid CD52. These findings elucidate a critical function of seminal fluid to suppress cellular immunity and facilitate reproduction.

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Publication Details

Journal
Frontiers in Immunology
Published
2024-12-16
DOI
https://doi.org/10.3389/fimmu.2024.1497889
Citations
2
Primary Topic
Reproductive System and Pregnancy
Type
article
Field-Weighted Citation Impact
0.48

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article

Soluble CD52 mediates immune suppression by human seminal fluid

Esther Bandala‐Sanchez, Jai Rautela, Moira K. O’Bryan, Natalie L. Stone et al.
2 citations
Frontiers in Immunology
Reproductive System and Pregnancy
0.48
article

Soluble CD52 mediates immune suppression by human seminal fluid

Esther Bandala‐Sanchez, Jai Rautela, Moira K. O’Bryan, Natalie L. Stone, Nicholas D. Huntington, Robert I. McLachlan, Leonard C. Harrison
article en
2 citations

Abstract

Seminal fluid provides for the carriage and nutrition of sperm, but also modulates immunity to prevent allo-rejection of sperm by the female. Immune suppression by seminal fluid has been associated with extracellular vesicles, originally termed prostasomes, which contain CD52, a glycosylated glycophosphoinositol-anchored peptide released from testicular epithelial cells. Previously, we reported that human T cell-derived CD52, bound to the danger-associated molecular pattern protein, high mobility group box 1 (HMGB1), suppresses T cell function via the inhibitory sialic acid-binding immunoglobulin-like lectin-10 (Siglec-10) receptor. Here we show that human seminal fluid contains high concentrations of CD52 complexed with HMGB1, which mediates T cell suppression indirectly via Siglec-7 on antigen-presenting cells. Proliferation of natural killer (NK) cells, which express Siglec-7 and play a key role in the immune defence of the uterus, was directly suppressed by seminal fluid CD52. These findings elucidate a critical function of seminal fluid to suppress cellular immunity and facilitate reproduction.

Frontiers in ImmunologyVol. 15
The University of Melbourne (AU), Walter and Eliza Hall Institute of Medical Research (AU), Hudson Institute of Medical Research (AU), Monash University (AU)
Medical Research Council, National Health and Medical Research Council
Zero hunger
Openalex Percentile: Top 33%
Reproductive System and Pregnancy
0.48
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