10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Age‐ and sex‐mediated differences in T lymphocyte populations of kidney transplant recipients

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          <p class="first" id="d4844634e200">Graft failure rates increase through childhood and adolescence, decline in adulthood, and are higher in female than male kidney transplant recipients (KTR) until middle age. We aimed to describe age- and sex-related differences in T-cell subsets among KTR to determine which differences may help to explain the differences in kidney graft failure rates. </p>

          Related collections

          Most cited references56

          • Record: found
          • Abstract: found
          • Article: not found

          Sex differences in immune responses

          Males and females differ in their immunological responses to foreign and self-antigens and show distinctions in innate and adaptive immune responses. Certain immunological sex differences are present throughout life, whereas others are only apparent after puberty and before reproductive senescence, suggesting that both genes and hormones are involved. Furthermore, early environmental exposures influence the microbiome and have sex-dependent effects on immune function. Importantly, these sex-based immunological differences contribute to variations in the incidence of autoimmune diseases and malignancies, susceptibility to infectious diseases and responses to vaccines in males and females. Here, we discuss these differences and emphasize that sex is a biological variable that should be considered in immunological studies.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Validation of a self-administered instrument to assess stage of adolescent development.

            Drawings were made from Tanner's photographs illustrating five stages of development each for male genitalia, testicular size, male pubic hair, female breasts, and female pubic hair. Forty-seven females and forty-eight males aged 12-16 years indicated on questionnaires which stage they were most like, and answered other questions related to their physical development. Afterwards they were examined by physicians who had not seen their answers. Pearson correlation coefficients were 0.6 or above for the physician's observations compared with the adolescents' answers for the drawings, with the exception of testicular size. Answers to questions concerning amount of underarm hair and general development also yielded high correlations.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              How sex and age affect immune responses, susceptibility to infections, and response to vaccination

              Do men die young and sick, or do women live long and healthy? By trying to explain the sexual dimorphism in life expectancy, both biological and environmental aspects are presently being addressed. Besides age-related changes, both the immune and the endocrine system exhibit significant sex-specific differences. This review deals with the aging immune system and its interplay with sex steroid hormones. Together, they impact on the etiopathology of many infectious diseases, which are still the major causes of morbidity and mortality in people at old age. Among men, susceptibilities toward many infectious diseases and the corresponding mortality rates are higher. Responses to various types of vaccination are often higher among women thereby also mounting stronger humoral responses. Women appear immune-privileged. The major sex steroid hormones exhibit opposing effects on cells of both the adaptive and the innate immune system: estradiol being mainly enhancing, testosterone by and large suppressive. However, levels of sex hormones change with age. At menopause transition, dropping estradiol potentially enhances immunosenescence effects posing postmenopausal women at additional, yet specific risks. Conclusively during aging, interventions, which distinctively consider the changing level of individual hormones, shall provide potent options in maintaining optimal immune functions.
                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Pediatric Transplantation
                Pediatric Transplantation
                Wiley
                1397-3142
                1399-3046
                February 2022
                September 27 2021
                February 2022
                : 26
                : 1
                Affiliations
                [1 ]Research Institute of the McGill University Health Centre Montreal Quebec Canada
                [2 ]Division of Experimental Medicine McGill University Montreal Quebec Canada
                [3 ]Division of Nephrology and Multi‐Organ Transplant Program McGill University Montreal Quebec Canada
                [4 ]Department of Epidemiology, Biostatistics and Occupational Health McGill University Montreal Quebec Canada
                [5 ]Département de Médecine Université de Montréal Montreal Quebec Canada
                [6 ]Centre de Recherche du Centre Hospitalier de l'Université de Montréal Montreal Quebec Canada
                [7 ]Département de Pédiatrie Université de Montréal Montreal Quebec Canada
                [8 ]Centre Hospitalier Universitaire Sainte‐Justine Montreal Quebec Canada
                [9 ]Department of Microbiology and Immunology McGill University Montreal Quebec Canada
                [10 ]Department of Pediatrics McGill University Montreal Quebec Canada
                Article
                10.1111/petr.14150
                34569133
                2cdd876e-6364-4d3b-b73d-b71abd319270
                © 2022

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

                History

                Comments

                Comment on this article