Rhesus isoimmunization: An underappreciated reproductive risk

Moses Obimbo, Kireki Omanwa
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 Rhesus isoimmunization can be prevented, but most Sub-Saharan African countries have not fully utilized these opportunities. As a result, many women are at risk due to poor medical records following potentially sensitizing events and a lack of access to crucial diagnostic and therapeutic commodities. These have significantly increased the difficulty of managing Rh-negative pregnancies (5).
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Abstract

In sub-Saharan Africa, pregnancy-related complications are a significant contributor to morbidity, mortality, and rising healthcare costs (1). The membrane of human red blood cells (RBCs) may contain the Rhesus (Rh) antigen. There are several types of Rh antigens but most important is the RhD antigen. Along the whole RhD protein, a group of conformation-dependent epitopes make up the D antigen. The most clinically significant blood group antigens that determine whether fetomaternal blood compatibility exists are the RhD and ABO systems (2). While the D-negative phenotype is linked to a deletion of RHD in most Caucasians, it is uncertain why the D antigen is not expressed other populations like the Japanese and Africans where it is linked to a grossly normal RHD (3). Accordingly, if a mother is Rh D-negative and the fetus is Rh D positive, she may produce antibodies through a process called RhD sensitization if she is exposed to fetal antigens. Sensitization is unlikely to damage the index fetus in normal conditions, but it may result in recurrent pregnancy losses, an infant with sensitized RBCs or to severe types of hemolytic disease of the newborn presenting with jaundice, anemia, developmental problems, or stillbirth (4). Rhesus isoimmunization can be prevented, but most Sub-Saharan African countries have not fully utilized these opportunities. As a result, many women are at risk due to poor medical records following potentially sensitizing events and a lack of access to crucial diagnostic and therapeutic commodities. These have significantly increased the difficulty of managing Rh-negative pregnancies (5). There has been a contentious suggestion for the universal prophylactic use of anti-D immunoglobulin in all pregnancies, including those following termination or ectopic pregnancy (6). We know that only a few at-risk women will profit from this strategy, which will unquestionably be highly expensive. However, there is no question that the Rh-negative pregnant population of Africa needs to have access to anti-D immunoglobulin on a global basis (7)(8). It follows that appropriate strategies should be instituted to effectively identify at-risk women and treat them accordingly (9). Leaders in obstetrics practice from various African countries met towards the end of last year to discuss the unmet need to address the burden of Rhesus disease. They noted that, despite being entirely preventable, Rhesus disease was identified as one of the roadblocks to achieving maternal universal health coverage. The team recommended all stakeholders to facilitate access to anti-D immunoglobulin and screening tools for widespread screening and treatment.
恒河猴等免疫:一种被低估的生殖风险
在撒哈拉以南非洲,妊娠相关并发症是发病率、死亡率和医疗费用上升的重要因素(1)。人红细胞(rbc)膜可能含有恒河猴(Rh)抗原。Rh抗原有几种类型,但最重要的是RhD抗原。沿着整个RhD蛋白,一组构象依赖的表位组成了D抗原。临床上最重要的血型抗原决定是否存在胎母血液相容性是RhD和ABO系统(2)。虽然在大多数白种人中,D阴性表型与RhD缺失有关,但尚不确定为什么D抗原在日本和非洲等其他人群中不表达,而在这些人群中,D抗原与非常正常的RhD有关(3)。因此,如果母亲是RhD阴性,而胎儿是RhD阳性,如果她接触到胎儿抗原,她可能会通过一种叫做RhD敏化的过程产生抗体。在正常情况下,致敏不太可能损害指标胎儿,但它可能导致反复妊娠丢失、致敏红细胞婴儿或新生儿出现黄疸、贫血、发育问题或死胎等严重溶血性疾病(4)。恒河猴等免疫是可以预防的,但大多数撒哈拉以南非洲国家没有充分利用这些机会。因此,许多妇女由于在可能发生的敏感事件之后的不良医疗记录以及无法获得关键的诊断和治疗商品而面临风险。这大大增加了处理rh阴性妊娠的难度(5)。有一个有争议的建议是在所有妊娠中普遍预防性使用抗d免疫球蛋白,包括那些终止妊娠或异位妊娠(6)。我们知道,只有少数高危妇女能从这种策略中获益,这无疑将是非常昂贵的。然而,毫无疑问,非洲rh阴性孕妇群体需要在全球范围内获得抗d免疫球蛋白(7)(8)。因此,应该制定适当的战略,有效地识别处于危险中的妇女,并对她们进行相应的治疗(9)。去年年底,来自非洲各国的产科实践领导人举行了会议,讨论了解决恒河猴病负担方面尚未满足的需求。他们指出,尽管恒河猴病是完全可以预防的,但仍被确定为实现孕产妇全民健康覆盖的障碍之一。该小组建议所有利益攸关方促进获得抗d免疫球蛋白和筛查工具,以进行广泛的筛查和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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