ABO Antibody Development, a New Look at a Very Old Question.
ABO Antibody Development, a New Look at a Very Old Question.
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ABO 抗体开发,一个非常古老的问题的新视角。
DOI:
10.1097/tp.0000000000004659
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发表时间:
2023
期刊:
影响因子:
6.2
通讯作者:
Zorn,Emmanuel
中科院分区:
文献类型:
--
作者:
Zorn,Emmanuel
The ABO blood group system is central to blood transfusion and transplantation medicine. The system is determined by the presence or absence of the A and B antigens on the surface of red blood cells and corresponding antibodies reactive to these antigens in the plasma. The ABO system was discovered more than a century ago by Karl Landsteiner, for which he received the Nobel Prize in Physiology or Medicine in 1930. 1 Yet to this day, the mechanism underlying the development of ABO antibodies remains obscure. Early studies suggested that immune reactions to the developing microbiota in early infancy generated cross-reactive antibodies to blood group antigens. 2 This common view explained why infants and toddlers up to 14 mo of age whose ABO antibodies are not fully developed can successfully receive ABO-incompatible heart transplants, as documented by Dr Lori West in a seminal study published in 2001. 3 However, although the timing of ABO antibody production is well documented, its dependency on exposure to microbial antigenic determinants is still hypothetical.The study by Dr Adam and his colleagues of the Edmonton group led by Dr West published in this issue of Transplantation sheds new light on this long-standing question. 4 The investigation, conducted in a mouse model, allowed the authors to address and essentially single out the contribution of CD4+ T cells, microbiota, and sex in the natural and induced development of antibodies to blood group antigen type A. The study first revealed that natural production of anti-A antibodies did not require CD4+ T cells. On the contrary, CD4+ T cells controlled and weakened the development of anti-A antibodies. This effect had previously been reported for anti-gal antibodies but not for anti-ABO antibodies. 5 Secondly and unexpectedly, the capacity of CD4+ T cells to mitigate the development of natural anti-A antibodies appeared more pronounced in females than in males. This intriguing effect of sex had