FCGR3B Antibody, HRP conjugated

1. SHP-2 is activated by CD16b crosslinking in neutrophils. PMID: 29137913
2. FCGR3B deficiency, due to copy number variations, may predispose individuals to eosinophilic granulomatosis with polyangiitis. PMID: 26684293
3. The FCGR3B NA1/NA1 genotype is associated with hypersensitivity reactions to adalimumab in Japanese patients with Rheumatoid Arthritis. PMID: 27830964
4. Research suggests an association between FCGR3B deletion and an increased risk of rheumatoid arthritis (RA) in a large cohort. PMID: 27995740
5. Association between Fc gamma Receptor IIIB genetic polymorphisms and susceptibility to severe malaria anemia in children in western Kenya. PMID: 28427365
6. CD16 and CD35 are essential for neutrophil internalization of M. tuberculosis, while HIV-1 infection negatively affects opsonophagocytosis. PMID: 27258232
7. There were no aberrations in FCGR3B allele/genotype frequencies in sarcoidosis patients compared to controls. PMID: 26801149
8. Results indicate that susceptibility to systemic lupus erythematosus was associated with the FCGR3B*01 allele, as well as with the FCGR3B*01/*01 and FCGR3B*01/*02 genotypes. PMID: 26946294
9. FcgammaRIIIB allelic distribution was similar among pediatric Guillain-Barre syndrome patients and controls. PMID: 27064330
10. Data show that cross-linking FcgammaRIIIb is responsible for NET formation by the human neutrophil PMID: 27034964
11. A meta-analysis indicated that low FCGR3B copy number increased susceptibility to autoimmune diseases. PMID: 26407570
12. FCGR3B copy number is related to systemic lupus and lupus nephritis susceptibility. PMID: 24673810
13. No relationship was found between the FCGR3B polymorphism and rheumatoid arthritis susceptibility. PMID: 26314337
14. This study compared the FCGR3B gene frequencies among 230 unrelated healthy Eastern Thai blood donors in Rayong hospital with previously published studies. PMID: 25626603
15. FcgammaRIIIb polymorphism is not associated with susceptibility to systemic lupus erythematosus in Brazilian patients. PMID: 24896836
16. In the Indian population, FCGR3B gene copy number varied significantly when compared to other populations worldwide. PMID: 25428402
17. A high copy number of FCGR3B is associated with psoriasis vulgaris in Han Chinese. PMID: 25012234
18. This suggests that FcgammaRIIIb signals in association with macrophage-1 Ag. PMID: 25024378
19. The frequencies of FCGR3B*1, FCGR3B*2, and FCGR3B*3 alleles in central Thai blood donors were 0.548, 0.452, and 0.004, respectively. PMID: 24205492
20. Copy number of polymorphisms in the FCGR3B gene is associated with ulcerative colitis. PMID: 23917248
21. The absolute risk of malaria decreased more rapidly with increasing antibody levels for Fc gamma receptor 3B 233AA/AC individuals compared with 233CC children. PMID: 23935200
22. The FCGR3B NA1/NA2 polymorphism may be associated with susceptibility to aggressive periodontitis. PMID: 23649770
23. This study concludes that gene copy number of FcgammaR2C and FcgammaR3B influences IVIG treatment response and predisposes individuals to Kawasaki disease, providing potential insights into understanding the mechanism of the FcgammaR gene family in the IVIG pathway. PMID: 23778324
24. Allele frequencies were determined in the blood donor population as follows: 0.318 for HNA-1a, 0.668 for HNA-1b, 0.014 for HNA-1c, 0.768 for HNA-3a, 0.232 for HNA-3b, 0.882 for HNA-4a, 0.118 for HNA-4b, 0.736 for HNA-5a and 0.264 for HNA-5b. PMID: 23398146
25. Higher CD16+ cytotoxic NK+T lymphocyte levels predict superior survival outcomes in patients with metastatic carcinoma. PMID: 23281059
26. Low copy number of the Fc-gamma receptor 3B gene FCGR3B is a risk factor for primary Sjogren's syndrome. PMID: 22942264
27. Studies indicate beta-defensins (DEFB4, DEFB103, DEFB104), chemokine ligand 3 like 1 (CCL3L1), Fc gamma receptor 3B (FCGR3B), and complement component C4 (C4) for copy number variation in disease association. PMID: 22837109
28. The FcgammaRIIIB-SH allotype (CTGAAA) containing the 233A-allele (in bold) was associated with protection from malaria. The FcgammaRIIIB-NA2*03 allotype (CTGCGA), a variant of the classical FcgammaRIIIB-NA2 (CTGCAA) was associated with susceptibility to malaria. PMID: 23049979
29. Findings suggest that impaired immune complex clearance arising from FCGR3B deficiency contributes to the pathology of systemic sclerosis, and FCGR3B copy number variation is a common risk factor for systemic autoimmunity. PMID: 22551723
30. CD14++CD16+ monocytes independently predicted cardiovascular events in subjects referred for elective coronary angiography. PMID: 22999728
31. A study indicates that a low copy number of the FCGR3B gene is associated with susceptibility to rheumatoid arthritis (RA). PMID: 22309893
32. The FcgammaRIIIB-NA1 variant, which confers higher affinity for IgG than the NA2 variant, is a determining factor for treatment response. PMID: 22565545
33. FCGR3B*1, FCGR3B*2 and FCGR3B*3 allele frequencies were respectively 0.347, 0.573 and 0.080 among Tunisians of sub-Saharan origin, 0.379, 0.591 and 0.030 among Tunisian blood donors and 0.318, 0.546 and 0.136 among the group from sub-Saharan Africa. PMID: 22512913
34. Both ADAM10 and ADAM17 could shed CD16b, but they possess differing preferences. ADAM10 is the main sheddase under ionomycin stimulation, while ADAM17 is the main sheddase under PMA stimulation. PMID: 22770404
35. The NA2/NA2 and/or NA2 allele may be risk factors for generalized aggressive periodontitis in the population of South India. PMID: 22167032
36. In this Brazilian FCGR3B*03(+) group, it was found that the inheritance of FCGR3B*03 took place by linkage to FCGR3B*02 or to FCGR3B*01. PMID: 21895673
37. FCGR3B DNA copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans. PMID: 21296850
38. Monocyte subsets have specialized roles during inflammation: CD16-positive monocytes might undergo an immediate innate immune response, whereas CD16-negative monocytes could have a major role as antigen presenting cells. PMID: 21937707
39. Research suggests that FcgammaRIIIb might not be a susceptibility gene for SLE and lupus nephritis. PMID: 20300756
40. Copy number associated with susceptibility to idiopathic pulmonary fibrosis. PMID: 21109729
41. IL-21 stimulates the production of IL-10 by CD4(+) T-cells. Secreted Il-10 maintains the expression of CD16 on monocytes. PMID: 21227406
42. The neutrophil responses to stimuli that engage FcGR3B and FcGR2A, namely the phagocytosis of human IgG-opsonized zymosan and the responses to heat-aggregated IgGs. PMID: 21123174
43. FcgammaRIIIb NA1/2 polymorphisms are associated with idiopathic pulmonary fibrosis disease susceptibility but not with disease progression. PMID: 20924590
44. This study highlights the complexity and poor characterization of the FCGR3B gene sequence, indicating that the design and interpretation of genotyping assays based on specific probe sequences must be performed with caution. PMID: 20957197
45. The FCGR3B NA1/NA1 genotype was found in 75% of the patients with infusion reactions and in only 37% of those without (p=0.01), whereas the FCGR3A 176F/V genotype was equally distributed in the patients with or without infusion reactions. PMID: 20980704
46. FcgammRIIA and FcgammaRIIIB are required for neutrophil mediated dermal epidermal separation in bullous pemphigoid. PMID: 20720565
47. Results, obtained by fitting logistic regression models, confirm the association of low copy number of FCGR3B with systemic lupus erythematosus. PMID: 20442749
48. Results of this study suggest that subjects carrying at least one copy of the FcgammaRIIIb-NA2 allele might be associated with susceptibility to aggressive periodontitis. PMID: 20041976
49. The primary involvement of the Fc gamma R IIIB NA2 allele is more likely involved with disease susceptibility of systemic lupus erythematosus. PMID: 20536598
50. Significant evidence for an association between copy number and rheumatoid arthritis was observed in the Dutch cohort but not in the two smaller cohorts (New Zealand and United Kingdom populations, respectively). PMID: 20472591

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HGNC: 3620

OMIM: 610665

KEGG: hsa:2215

STRING: 9606.ENSP00000294800

UniGene: Hs.372679