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Makale detayı · 2010 · article

Revisiting Human IL 12R 1 Deficiency

Dergi Medicine ISSN kaydı başka bir dergiye işaret ediyor; ad YÖKSİS kaydından.
ISSN0025-7974
YÖKSİS OpenAlex Açık erişim · green Üst %10
Yıl2010
Atıf394OpenAlex
Atıf361Semantic Scholar · 7 etkili
Yüzdelik%98,9
FWCI10,51,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıMedicine
  • Katalog eşleşmesi (ISSN)Medicine (United States)
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Interleukin-12 receptor β1 (IL-12Rβ1) deficiency is the most common form of Mendelian susceptibility to mycobacterial disease (MSMD). We undertook an international survey of 141 patients from 102 kindreds in 30 countries. Among 102 probands, the first infection occurred at a mean age of 2.4 years. In 78 patients, this infection was caused by Bacille Calmette-Guérin (BCG; n = 65), environmental mycobacteria (EM; also known as atypical or nontuberculous mycobacteria) (n = 9) or Mycobacterium tuberculosis (n = 4). Twenty-two of the remaining 24 probands initially presented with nontyphoidal, extraintestinal salmonellosis. Twenty of the 29 genetically affected sibs displayed clinical signs (69%); however 8 remained asymptomatic (27%). Nine nongenotyped sibs with symptoms died. Recurrent BCG infection was diagnosed in 15 cases, recurrent EM in 3 cases, recurrent salmonellosis in 22 patients. Ninety of the 132 symptomatic patients had infections with a single microorganism. Multiple infections were diagnosed in 40 cases, with combined mycobacteriosis and salmonellosis in 36 individuals. BCG disease strongly protected against subsequent EM disease (p = 0.00008). Various other infectious diseases occurred, albeit each rarely, yet candidiasis was reported in 33 of the patients (23%). Ninety-nine patients (70%) survived, with a mean age at last follow-up visit of 12.7 years ± 9.8 years (range, 0.5-46.4 yr). IL-12Rβ1 deficiency is characterized by childhood-onset mycobacteriosis and salmonellosis, rare recurrences of mycobacterial disease, and more frequent recurrence of salmonellosis. The condition has higher clinical penetrance, broader susceptibility to infections, and less favorable outcome than previously thought. Abbreviations: BCG = Bacille Calmette-Guérin, CI = confidence interval, EBV-B cell lines = Epstein-Barr virus-transformed lymphoblastoid cell lines, ELISA = enzyme-linked immunosorbent assay, EM= environmental mycobacteria (nontuberculous mycobacteria), FBS = fetal bovine serum, FD = fibronectin domain, IFNGR = interferon-γ receptor, IL12B = interleukin-12B, IL-12Rβ1 = interleukin-12 receptor beta 1 chain, MSMD = Mendelian susceptibility tomycobacterial disease, NEMO = nuclear factor-κB essential modulator, PBS = phosphate-buffered saline, PCR = polymerase chain reaction, PHA = phytohemagglutinin, PR = present report, STAT1 = Signal transducer and activator of transcription 1.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

394atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 66 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2016 Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotypeAtıf 581 · OpenAlex
  2. 2015 Human TYK2 deficiency Mycobacterial and viral infections without hyper IgE syndromeAtıf 369 · OpenAlex
  3. 2012 Functional STAT3 deficiency compromises the generation of human T follicular helper cellsAtıf 318 · OpenAlex
  4. 2016 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 226 · OpenAlex
  5. 2015 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 226 · OpenAlex
  6. 2015 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 226 · OpenAlex
  7. 2015 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 224 · OpenAlex
  8. 2015 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 224 · OpenAlex
  9. 2015 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 224 · OpenAlex
  10. 2015 Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodAtıf 224 · OpenAlex

Yazarlar

3
  1. GÜZİDE AKSU 1
  2. AYPER SOMER İSTANBUL ÜNİVERSİTESİ 2
  3. YILDIZ CAMCIOĞLU 3