The non-receptor tyrosine phosphatase PTPN22 has a vital function in inhibiting antigen-receptor signaling in T cells, while polymorphisms in the PTPN22 gene are important risk alleles in human autoimmune diseases. We recently reported that a key physiological function of PTPN22 was to prevent naïve T cell activation and effector cell responses in response to low affinity antigens. PTPN22 also has a more general role in limiting T cell receptor-induced proliferation. Here we present new data emphasizing this dual function for PTPN22 in T cells. Furthermore, we show that T cell activation modulates the expression of PTPN22 and additional inhibitory phosphatases. We discuss the implication of these findings for our understanding of the roles ...
The tyrosine phosphatase PTPN22 regulates T cell receptor signaling. In this issue of Immunity, Wang...
Many autoimmune diseases exhibit familial aggregation, indicating that they have genetic determinant...
The PTPN22R620W single nucleotide polymorphism increases the risk of developing multiple autoimmune ...
The non-receptor tyrosine phospha-tase PTPN22 has a vital function in inhibiting antigen-receptor si...
The cytoplasmic phosphatase PTPN22 (protein tyrosine phosphatase nonreceptor type 22) plays a key ro...
The cytoplasmic phosphatase PTPN22 (protein tyrosine phosphatase nonreceptor type 22) plays a key ro...
A single nucleotide polymorphism, C1858T, in the gene encoding the protein tyrosine phosphatase nonr...
T cells must be tolerant of self antigens to avoid autoimmunity but responsive to foreign antigens t...
A number of polymorphisms in immune‐regulatory genes have been identified as risk factors for the de...
T cells must be tolerant of self antigens to avoid autoimmunity but responsive to foreign antigens t...
The cytoplasmic phosphatase, protein tyrosine phosphatase nonreceptor type 22 (PTPN22), is a negativ...
<div><p>The PTPN22<sup>R620W</sup> single nucleotide polymorphism increases the risk of developing m...
A missense C1858T single nucleotide polymorphism within PTPN22 is a strong genetic risk factor for t...
AbstractA cDNA of PTPN2 encoding for T-cell protein tyrosine phosphate (TC-PTP) was isolated and cha...
The protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene located on chromosomes 1p 13.3–1...
The tyrosine phosphatase PTPN22 regulates T cell receptor signaling. In this issue of Immunity, Wang...
Many autoimmune diseases exhibit familial aggregation, indicating that they have genetic determinant...
The PTPN22R620W single nucleotide polymorphism increases the risk of developing multiple autoimmune ...
The non-receptor tyrosine phospha-tase PTPN22 has a vital function in inhibiting antigen-receptor si...
The cytoplasmic phosphatase PTPN22 (protein tyrosine phosphatase nonreceptor type 22) plays a key ro...
The cytoplasmic phosphatase PTPN22 (protein tyrosine phosphatase nonreceptor type 22) plays a key ro...
A single nucleotide polymorphism, C1858T, in the gene encoding the protein tyrosine phosphatase nonr...
T cells must be tolerant of self antigens to avoid autoimmunity but responsive to foreign antigens t...
A number of polymorphisms in immune‐regulatory genes have been identified as risk factors for the de...
T cells must be tolerant of self antigens to avoid autoimmunity but responsive to foreign antigens t...
The cytoplasmic phosphatase, protein tyrosine phosphatase nonreceptor type 22 (PTPN22), is a negativ...
<div><p>The PTPN22<sup>R620W</sup> single nucleotide polymorphism increases the risk of developing m...
A missense C1858T single nucleotide polymorphism within PTPN22 is a strong genetic risk factor for t...
AbstractA cDNA of PTPN2 encoding for T-cell protein tyrosine phosphate (TC-PTP) was isolated and cha...
The protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene located on chromosomes 1p 13.3–1...
The tyrosine phosphatase PTPN22 regulates T cell receptor signaling. In this issue of Immunity, Wang...
Many autoimmune diseases exhibit familial aggregation, indicating that they have genetic determinant...
The PTPN22R620W single nucleotide polymorphism increases the risk of developing multiple autoimmune ...