| Literature DB >> 34309860 |
Layana Pachêco de Araújo Albuquerque1, Amanda Miranda da Silva2,3, Francisca Miriane de Araújo Batista4, Ingridi de Souza Sene3, Dorcas Lamounier Costa5, Carlos Henrique Nery Costa6.
Abstract
The differences in morbidity and mortality patterns and life expectancy between the sexes are well established in different infectious and parasitic conditions, such as in leishmaniases, in which biological, genetic, sexual and hormonal variations can modulate the immune response indicating greater infectivity, prevalence and clinical severity in men. In this regard, in seeking the understanding of factors related to protection and susceptibility to infection, this review aimed to discuss the influence of sex hormones on the immune response to leishmaniases. In the literature, sex hormone variations promote differences in the innate, humoral and cell-mediated immune response, leading to greater susceptibility, mortality and complications in males. Epidemiological estimates confirm these results, showing a predominance of the disease, in its different clinical forms, in men and suggesting that sexual variations influence immunomodulatory mechanisms since the prevalence of cases comprises the post-puberty and adulthood period. In this perspective, the action of sex hormones has been investigated in different clinical models, highlighting the potential of testosterone in immunosuppression, given its association with greater susceptibility and poor control of parasite load and the induction of cell apoptosis and attenuation of pro-inflammatory signalling pathways. Therefore, hormonal variations influence the immune response among males and females against leishmaniases, in which androgens may present immunosuppressive potential, while steroids present immunomodulatory characteristics.Entities:
Keywords: immune response; infectious diseases; leishmaniases; sex bias; sex hormones
Year: 2021 PMID: 34309860 DOI: 10.1111/pim.12874
Source DB: PubMed Journal: Parasite Immunol ISSN: 0141-9838 Impact factor: 2.280