Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Query: UMLS:C0024312 (
lymphopenia
)
4,859
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
B-cell survival depends on signals induced by B-cell activating factor (BAFF) binding to its receptor (
BAFF-R
). In mice, mutations in BAFF or
BAFF-R
cause B-cell
lymphopenia
and antibody deficiency. Analyzing
BAFF-R
expression and BAFF-binding to B cells in common variable immunodeficiency (CVID) patients, we identified two siblings carrying a homozygous deletion in the
BAFF-R
gene. Removing most of the
BAFF-R
transmembrane part, the deletion precludes
BAFF-R
expression. Without
BAFF-R
, B-cell development is arrested at the stage of transitional B cells and the numbers of all subsequent B-cell stages are severely reduced. Both siblings have lower IgG and IgM serum levels but, unlike most CVID patients, normal IgA concentrations. They also did not mount a T-independent immune response against pneumococcal cell wall polysaccharides but only one
BAFF-R
-deficient sibling developed recurrent infections. Therefore, deletion of the
BAFF-R
gene in humans causes a characteristic immunological phenotype but it does not necessarily lead to a clinically manifest immunodeficiency.
...
PMID:B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans. 1966 84
The BAFF-receptor (BAFFR) is encoded by the
TNFRSF13C
gene and is one of the main pro-survival receptors in B cells. Its function is impressively documented in humans by a homozygous deletion within exon 2, which leads to an almost complete block of B cell development at the stage of immature/transitional B cells. The resulting immunodeficiency is characterized by B-
lymphopenia
, agammaglobulinemia, and impaired humoral immune responses. However, different from mutations affecting pathway components coupled to B cell antigen receptor (BCR) signaling, BAFFR-deficient B cells can still develop into IgA-secreting plasma cells. Therefore, BAFFR deficiency in humans is characterized by very few circulating B cells, very low IgM and IgG serum concentrations but normal or high IgA levels.
...
PMID:BAFF and BAFF-Receptor in B Cell Selection and Survival. 3034 34