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The Human Penis Is a Genuine Immunological Effector Site
Alexis Sennepin1,2,3, Fernando Real1,2,3, Marine Duvivier1,2,3
1Laboratory of Mucosal Entry of HIV-1 and Mucosal Immunity, Department of Infection, Immunity and Inflammation, Cochin Institute, INSERM, Paris, France.
Frontiers in Immunology
|January 10, 2018
Summary
The human penis contains immune cells like B, T, and NK cells, indicating it
Area of Science:
- Immunology
- Urology
- Infectious Diseases
Background:
- The human penis serves as a primary entry point for various pathogens.
- Understanding the penile immune system is crucial for developing effective local vaccines against infections.
- Mechanisms of penile immune response induction remain largely unknown.
Purpose of the Study:
- To characterize the mucosal immune cells within different regions of the human penis.
- To investigate the presence and phenotype of B, T, and NK cells in penile tissues.
- To determine the immunological activity and effector potential of the human penile tissue.
Main Methods:
- Descriptive study utilizing multiparametric flow cytometry and immunohistochemistry.
- Analysis of immune cell populations (B, T, NK cells) in urethral, fossa, and glans penile tissues.
- Assessment of cell phenotypes, cytokine secretion, and homing receptor expression.
Main Results:
- Memory B lymphocytes, CD138+ plasma cells, CD4+, and CD8+ T lymphocytes are present in all penile compartments.
- CD56dim NK cells expressing NKp44 and CD16 are found, capable of secreting IL-17 and IL-22.
- While immune cell content is comparable across regions, the glans shows higher numbers of activated NK and effector CD8+ T cells, suggesting superior effector function.
Conclusions:
- The human penis is an immunologically active tissue with the cellular components necessary for mounting an effective immune response.
- It functions as a mucosal effector site, relevant for designing vaccines against sexually transmitted infections.
- Penile immune cell characterization provides a foundation for future strategies targeting mucosal immunity.
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