Primary immunodeficiency Diseases: Current and Emerging Therapeutics

被引:35
作者
Marciano, Beatriz E. [1 ]
Holland, Steven M. [1 ]
机构
[1] NIAID, Lab Clin Infect Dis, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
关键词
immunodeficiency; immune modulation; chronic granulomatous disease; leukocyte adhesion deficiency; interferon gamma; CHRONIC GRANULOMATOUS-DISEASE; IMMUNE-DEFICIENCY; INTERFERON-GAMMA; VIRUS INFECTION; T-LYMPHOCYTES; AUTOIMMUNE; INTERLEUKIN-2; RITUXIMAB; THERAPY; COMMON;
D O I
10.3389/fimmu.2017.00937
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primary immunodeficiency diseases (PID) result from defects in genes affecting the immune and other systems in many and varied ways (1, 2). Until the last few years, treatments have been largely supportive, with the exception of bone marrow transplantation. However, recent advances in immunobiology, genetics, and the explosion of discovery and commercialization of biologic modifiers have drastically altered the landscape and opportunities in clinical immunology. Therapeutic options and life expectancy of PID patients have also improved dramatically, in large part as a result of better prevention and treatment of infections as well as better understanding and treatment of autoimmune complications (3). As early-life infection-related mortality declines we should anticipate the emergence of other conditions that were previously not appreciated, including malignancies and degenerative disorders unmasked by increasing longevity (4). The genomic revolution has identified literally hundreds of new genetic etiologies of immune dysfunction, many of which are or will soon be eligible for targeted therapies. These emerging immunomodulatory agents represent new therapeutic options in PIDs (5).
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页数:6
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共 55 条
[51]   RECOMBINANT HUMAN INTERFERON-GAMMA IN PATIENTS WITH CHRONIC GRANULOMATOUS-DISEASE - EUROPEAN FOLLOW-UP-STUDY [J].
WEENING, RS ;
LEITZ, GJ ;
SEGER, RA .
EUROPEAN JOURNAL OF PEDIATRICS, 1995, 154 (04) :295-298
[52]   Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation [J].
Weinacht, Katja G. ;
Charbonnier, Louis-Marie ;
Alroqi, Fayhan ;
Plant, Ashley ;
Qiao, Qi ;
Wu, Hao ;
Ma, Clement ;
Torgerson, Troy R. ;
Rosenzweig, Sergio D. ;
Fleisher, Thomas A. ;
Notarangelo, Luigi D. ;
Hanson, Imelda C. ;
Forbes, Lisa R. ;
Chatila, Talal A. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 139 (05) :1629-+
[53]   Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition [J].
Xing, Luzhou ;
Dai, Zhenpeng ;
Jabbari, Ali ;
Cerise, Jane E. ;
Higgins, Claire A. ;
Gong, Weijuan ;
de Jong, Annemieke ;
Harel, Sivan ;
DeStefano, Gina M. ;
Rothman, Lisa ;
Singh, Pallavi ;
Petukhova, Lynn ;
Mackay-Wiggan, Julian ;
Christiano, Angela M. ;
Clynes, Raphael .
NATURE MEDICINE, 2014, 20 (09) :1043-1049
[54]   Targeting Th17 Effector Cytokines for the Treatment of Autoimmune Diseases [J].
Yamagata, Tetsuya ;
Skepner, Jill ;
Yang, Jianfei .
ARCHIVUM IMMUNOLOGIAE ET THERAPIAE EXPERIMENTALIS, 2015, 63 (06) :405-414
[55]   Use of sirolimus in IPEX and IPEX-like children [J].
Yong, Pierre L. ;
Russo, Pierre ;
Sullivan, Kathleen E. .
JOURNAL OF CLINICAL IMMUNOLOGY, 2008, 28 (05) :581-587