PMID- 12969506 OWN - NLM STAT- MEDLINE DCOM- 20040601 LR - 20221207 IS - 1471-2350 (Electronic) IS - 1471-2350 (Linking) VI - 4 DP - 2003 Sep 12 TI - Association of HLA class I with severe acute respiratory syndrome coronavirus infection. PG - 9 AB - BACKGROUND: The human leukocyte antigen (HLA) system is widely used as a strategy in the search for the etiology of infectious diseases and autoimmune disorders. During the Taiwan epidemic of severe acute respiratory syndrome (SARS), many health care workers were infected. In an effort to establish a screening program for high risk personal, the distribution of HLA class I and II alleles in case and control groups was examined for the presence of an association to a genetic susceptibly or resistance to SARS coronavirus infection. METHODS: HLA-class I and II allele typing by PCR-SSOP was performed on 37 cases of probable SARS, 28 fever patients excluded later as probable SARS, and 101 non-infected health care workers who were exposed or possibly exposed to SARS coronavirus. An additional control set of 190 normal healthy unrelated Taiwanese was also used in the analysis. RESULTS: Woolf and Haldane Odds ratio (OR) and corrected P-value (Pc) obtained from two tails Fisher exact test were used to show susceptibility of HLA class I or class II alleles with coronavirus infection. At first, when analyzing infected SARS patients and high risk health care workers groups, HLA-B*4601 (OR = 2.08, P = 0.04, Pc = n.s.) and HLA-B*5401 (OR = 5.44, P = 0.02, Pc = n.s.) appeared as the most probable elements that may be favoring SARS coronavirus infection. After selecting only a "severe cases" patient group from the infected "probable SARS" patient group and comparing them with the high risk health care workers group, the severity of SARS was shown to be significantly associated with HLA-B*4601 (P = 0.0008 or Pc = 0.0279). CONCLUSIONS: Densely populated regions with genetically related southern Asian populations appear to be more affected by the spreading of SARS infection. Up until recently, no probable SARS patients were reported among Taiwan indigenous peoples who are genetically distinct from the Taiwanese general population, have no HLA-B* 4601 and have high frequency of HLA-B* 1301. While increase of HLA-B* 4601 allele frequency was observed in the "Probable SARS infected" patient group, a further significant increase of the allele was seen in the "Severe cases" patient group. These results appeared to indicate association of HLA-B* 4601 with the severity of SARS infection in Asian populations. Independent studies are needed to test these results. FAU - Lin, Marie AU - Lin M AD - Transfusion Medicine Laboratory, Mackay Memorial Hospital, Taipei, Taiwan. marilin@ms2.mmh.org.tw FAU - Tseng, Hsiang-Kuang AU - Tseng HK FAU - Trejaut, Jean A AU - Trejaut JA FAU - Lee, Hui-Lin AU - Lee HL FAU - Loo, Jun-Hun AU - Loo JH FAU - Chu, Chen-Chung AU - Chu CC FAU - Chen, Pei-Jan AU - Chen PJ FAU - Su, Ying-Wen AU - Su YW FAU - Lim, Ken Hong AU - Lim KH FAU - Tsai, Zen-Uong AU - Tsai ZU FAU - Lin, Ruey-Yi AU - Lin RY FAU - Lin, Ruey-Shiung AU - Lin RS FAU - Huang, Chun-Hsiung AU - Huang CH LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20030912 PL - England TA - BMC Med Genet JT - BMC medical genetics JID - 100968552 RN - 0 (HLA-A Antigens) RN - 0 (HLA-B Antigens) RN - 0 (HLA-B*46:01 antigen) RN - 0 (HLA-DR Antigens) RN - 0 (HLA-DRB1 Chains) RN - 0 (Histocompatibility Antigens Class I) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Alleles MH - Female MH - Gene Frequency MH - Genetic Testing/methods MH - HLA-A Antigens/genetics MH - HLA-B Antigens/genetics MH - HLA-DR Antigens/genetics MH - HLA-DRB1 Chains MH - Histocompatibility Antigens Class I/*genetics MH - Histocompatibility Testing/methods MH - Humans MH - Immunity, Innate/genetics/immunology MH - Male MH - Middle Aged MH - Odds Ratio MH - Polymerase Chain Reaction/methods MH - Severe acute respiratory syndrome-related coronavirus/immunology MH - Severe Acute Respiratory Syndrome/diagnosis/genetics/*immunology MH - Taiwan PMC - PMC212558 EDAT- 2003/09/13 05:00 MHDA- 2004/06/02 05:00 PMCR- 2003/09/12 CRDT- 2003/09/13 05:00 PHST- 2003/06/26 00:00 [received] PHST- 2003/09/12 00:00 [accepted] PHST- 2003/09/13 05:00 [pubmed] PHST- 2004/06/02 05:00 [medline] PHST- 2003/09/13 05:00 [entrez] PHST- 2003/09/12 00:00 [pmc-release] AID - 1471-2350-4-9 [pii] AID - 10.1186/1471-2350-4-9 [doi] PST - epublish SO - BMC Med Genet. 2003 Sep 12;4:9. doi: 10.1186/1471-2350-4-9.