Secondary antibody deficiencies

被引:52
作者
Dhalla, Fatima [1 ]
Misbah, Siraj A. [1 ]
机构
[1] Oxford Univ Hosp NHS Trust, Dept Clin Immunol, Oxford, England
基金
英国惠康基金;
关键词
drugs; lymphoproliferative disease; monoclonal antibodies; secondary antibody deficiency; CHRONIC LYMPHOCYTIC-LEUKEMIA; IMMUNOGLOBULIN REPLACEMENT THERAPY; INTRAVENOUS IMMUNE GLOBULIN; GIANT-CELL ARTERITIS; MULTIPLE-MYELOMA; MYOTONIC-DYSTROPHY; INTESTINAL LYMPHANGIECTASIA; MONOCLONAL GAMMOPATHY; RANDOMIZED-TRIAL; T-CELLS;
D O I
10.1097/ACI.0000000000000215
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose of review Antibody deficiency can occur in the context of primary immune deficiency due to inherited genetic defects or secondary to a variety of causes. This review aims to summarize current data concerning the causes of secondary antibody deficiency and where possible evidence regarding the use of prophylactic replacement immunoglobulin. Recent findings Advances in immune-mediated therapies ranging from monoclonal antibodies to novel B-cell- targeted therapeutics are responsible for an expansion in the possible iatrogenic causes of antibody deficiency. Summary Causes of secondary antibody deficiency include B- cell lymphoproliferative disease, notably chronic lymphocytic leukaemia and multiple myeloma, protein losing states, disorders of lymphatic circulation, increased immunoglobulin catabolism and a growing number of therapeutic agents. At-risk patients should be closely monitored for the development of hypogammaglobulinaemia, B- cell function should be defined where appropriate with specific antibody responses to immunization antigens and where there is a significant burden of infections patients should be treated with prophylactic antibiotics and/or replacement immunoglobulin.
引用
收藏
页码:505 / 513
页数:9
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