TY - CHAP
T1 - Genetics of Sex Differences in Immunity
AU - Gal-Oz, Shani T.
AU - Shay, Tal
N1 - Publisher Copyright:
© The Author(s), under exclusive license to Springer Nature Switzerland AG. 2023.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Women have a stronger immune response and a higher frequency of most autoimmune diseases than men. While much of the difference between men and women is due to the effect of gonadal hormones, genetic differences play a major role in the difference between the immune response and disease frequencies in women and men. Here, we focus on the immune differences between the sexes that are not downstream of the gonadal hormones. These differences include the gene content of the sex chromosomes, the inactivation of chromosome X in women, the consequences of non-random X inactivation and escape from inactivation, and the states that are uniquely met by the immune system of women—pregnancy, birth, and breast feeding. While these female-specific states are temporary and involve gonadal hormonal changes, they may leave a long-lasting footprint on the health of women, for example, by fetal cells that remain in the mother’s body for decades. We also briefly discuss the immune phenotype of congenital sex chromosomal aberrations and experimental models that enable hormonal and the non-hormonal effects of the sex chromosomes to be disentangled. The increasing human life expectancy lengthens the period during which gonadal hormones levels are reduced in both sexes. A better understanding of the non-hormonal effects of sex chromosomes thus becomes more important for improving the life quality during that period.
AB - Women have a stronger immune response and a higher frequency of most autoimmune diseases than men. While much of the difference between men and women is due to the effect of gonadal hormones, genetic differences play a major role in the difference between the immune response and disease frequencies in women and men. Here, we focus on the immune differences between the sexes that are not downstream of the gonadal hormones. These differences include the gene content of the sex chromosomes, the inactivation of chromosome X in women, the consequences of non-random X inactivation and escape from inactivation, and the states that are uniquely met by the immune system of women—pregnancy, birth, and breast feeding. While these female-specific states are temporary and involve gonadal hormonal changes, they may leave a long-lasting footprint on the health of women, for example, by fetal cells that remain in the mother’s body for decades. We also briefly discuss the immune phenotype of congenital sex chromosomal aberrations and experimental models that enable hormonal and the non-hormonal effects of the sex chromosomes to be disentangled. The increasing human life expectancy lengthens the period during which gonadal hormones levels are reduced in both sexes. A better understanding of the non-hormonal effects of sex chromosomes thus becomes more important for improving the life quality during that period.
KW - Chromosome X inactivation
KW - Fetal microchimerism
KW - Immune sexual dimorphism
KW - Sex chromosome aberrations
KW - Sex chromosomes
UR - http://www.scopus.com/inward/record.url?scp=85170488887&partnerID=8YFLogxK
U2 - 10.1007/978-3-031-35139-6_1
DO - 10.1007/978-3-031-35139-6_1
M3 - Chapter
C2 - 37695423
AN - SCOPUS:85170488887
T3 - Current Topics in Microbiology and Immunology
SP - 1
EP - 19
BT - Current Topics in Microbiology and Immunology
PB - Springer Science and Business Media Deutschland GmbH
ER -