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物以类聚:常见可变免疫缺陷。

Birds of a feather: Common variable immune deficiencies.

机构信息

Division of Allergy and Immunology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Department of Pediatrics, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

Division of Asthma, Allergy and Immunology, Department of Medicine, University of Virginia, Charlottesville, Virginia.

出版信息

Ann Allergy Asthma Immunol. 2019 Nov;123(5):461-467. doi: 10.1016/j.anai.2019.07.027. Epub 2019 Aug 2.

Abstract

OBJECTIVE

To update the reader on recently proposed common variable immune deficiency (CVID) diagnostic criteria, newly uncovered CVID pathobiology, freshly identified CVID-related genes, and novel CVID therapies.

DATA SOURCES

PubMed Central.

STUDY SELECTIONS

We selected 60 clinical and translational research articles that have shaped CVID diagnostic criteria, introduced personalized therapies, and advanced our understanding of CVID biology and genetics. We have incorporated recent articles and older published work that are foundational to the modern understanding of this protean disease.

RESULTS

CVID has proven to be a heterogenous group of antibody deficiency diseases driven by defects in diverse biologic processes, including B-cell development, activation, tolerance, class-switch recombination, somatic hypermutation, and lymphoproliferation. Recent genetic advances have enabled identification of several CVID-related gene defects that may contribute to patients' infectious and noninfectious symptoms.

CONCLUSION

Improved understanding of the aberrant biologic processes that drive CVID and the disease's genetic basis may be useful in directing therapeutic decisions, especially in cases complicated by autoimmune, lymphoproliferative, and inflammatory features.

摘要

目的

使读者了解最近提出的常见可变免疫缺陷(CVID)诊断标准、新发现的 CVID 病理生物学、新确定的 CVID 相关基因以及新的 CVID 治疗方法。

资料来源

PubMed Central。

研究选择

我们选择了 60 篇临床和转化研究文章,这些文章塑造了 CVID 的诊断标准、引入了个性化治疗方法,并加深了我们对 CVID 生物学和遗传学的理解。我们纳入了最近的文章和对该复杂疾病具有基础性的旧有发表工作。

结果

CVID 已被证明是一组异质性抗体缺陷疾病,由多种生物学过程的缺陷驱动,包括 B 细胞发育、激活、耐受、类别转换重组、体细胞高频突变和淋巴增殖。最近的遗传进展使我们能够确定几个可能导致患者感染和非感染症状的 CVID 相关基因缺陷。

结论

对导致 CVID 的异常生物学过程及其遗传基础的更好理解可能有助于指导治疗决策,特别是在伴有自身免疫、淋巴增殖和炎症特征的情况下。

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