TY - JOUR
T1 - Susceptibility of HLA-B27 transgenic mice to Yersinia enterocolitica infection
AU - Nickerson, Cheryl L.
AU - Luthra, Harvinder S.
AU - Savarirayan, Suresh
AU - David, Chella S.
N1 - Funding Information:
This work was supported by grants from the National Institute of Arthritis and Metabolic Diseases (AR-39875), the Minnesota Chapter of the Arthritis Foundation, and the Mayo Foundation. C.L.N. was supported by an NIH training grant (CA-09127).
PY - 1990/8
Y1 - 1990/8
N2 - The majority of patients with reactive arthritis have the major histocompatibility complex class I gene HLA-B27. The development of arthritis in these patients often occurs following infection with one of several enteric bacteria, including Yersinia enterocolitica. In this study, transgenic mice expressing HLA-B27 and their negative full sibs were infected intravenously with Yersinia enterocolitica 0:8 WA in an attempt to develop an experimental model of reactive arthritis. To date, no reactive arthritis has been observed; however, a significantly higher incidence of paralysis was observed in the HLA-B27+ transgenic mice. Injection of 105 organisms induced hind limb paralysis in 8 out of 30 of the HLA-B27 transgenic mice (27%) and in only 1 of the 24 negative siblings (4%). Paralysis occurred in 14 out of 30 HLA-B27+ mice (47%) at a dose of 104 organisms. Only 2 of the 25 negative siblings (8%) were affected at this dose. Paraspinal abscesses were found in all of the paralyzed animals. At the 104 dose most of the HLA-B27+ mice (70%) succumbled to the disease within 4 weeks, while the mortality in their B27- full sibs was less than 10%. Thus, HLA-B27 transgenic mice have higher mortality and morbidity from infection with Y. enterocolitica 0:8 WA than corresponding HLA-B27- littermates.
AB - The majority of patients with reactive arthritis have the major histocompatibility complex class I gene HLA-B27. The development of arthritis in these patients often occurs following infection with one of several enteric bacteria, including Yersinia enterocolitica. In this study, transgenic mice expressing HLA-B27 and their negative full sibs were infected intravenously with Yersinia enterocolitica 0:8 WA in an attempt to develop an experimental model of reactive arthritis. To date, no reactive arthritis has been observed; however, a significantly higher incidence of paralysis was observed in the HLA-B27+ transgenic mice. Injection of 105 organisms induced hind limb paralysis in 8 out of 30 of the HLA-B27 transgenic mice (27%) and in only 1 of the 24 negative siblings (4%). Paralysis occurred in 14 out of 30 HLA-B27+ mice (47%) at a dose of 104 organisms. Only 2 of the 25 negative siblings (8%) were affected at this dose. Paraspinal abscesses were found in all of the paralyzed animals. At the 104 dose most of the HLA-B27+ mice (70%) succumbled to the disease within 4 weeks, while the mortality in their B27- full sibs was less than 10%. Thus, HLA-B27 transgenic mice have higher mortality and morbidity from infection with Y. enterocolitica 0:8 WA than corresponding HLA-B27- littermates.
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U2 - 10.1016/0198-8859(90)90033-L
DO - 10.1016/0198-8859(90)90033-L
M3 - Article
C2 - 2391253
AN - SCOPUS:0025311556
SN - 0198-8859
VL - 28
SP - 382
EP - 396
JO - Human Immunology
JF - Human Immunology
IS - 4
ER -