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| Official Symbol of Gene | HLA-DRB4 |
| Species | Homo sapiens |
| Entrez Gene ID | 3126 |
| Official Full Name | major histocompatibility complex, class II, DR beta 4 |
| Also known as | DR4; DRB4; HLA-DRB; HLA-DR4B; HLA-DRB4* |
| Gene Type | protein coding |
| dbXrefs | HGNC:HGNC:4952 |
| Map Location | 6p21.3 |
| Detected Sample | Peripheral blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 13cases/13controls |
| Pubmed ID | 10653315 |
| Year | 1999 |
| Title | Cytokine production in patients carrying multiple sclerosis-linked HLA-DR alleles |
| Expression | up-regulation |
| Risk type | Disease risk |
| Result | We found normal levels of TNFα production by in vitro activated HLA-DR3+ and HLA-DR2+ lymphoid cells; in contrast, HLA-DR4+ MS patients produced significantly higher amounts of TNFα than healthy controls, and DR3+ and DR2+ patients. IFNγ, IL-10, and IL-4 levels did not differ significantly between the three groups of patients. |
| Mechanism/Pathway | TNF alleles reside within the class III region of the MHC and may be considered as candidate genes when studying HLA-linked MS susceptibility. The substitution of guanine (TNF1 allele) with adenosine (TNF2 allele) at position –308 of the polymorphic TNFα promoter region has been found to induce in vitro hyperproduction of TNFα from activated lymphoid cells [2, 14]. Although in contradiction to this, some authors suggest that HLA alleles associated with MS [3, 15], insulin-dependent diabetes mellitus [12], and systemic lupus erythematosus [6] may play a role of marker of linkage with polymorphic alleles predisposing to TNFα hyperproduction, raising the strong possibility that mononuclear cell cytokine production is controlled by the MHC genotype. |

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