TY - JOUR
T1 - Human parvovirus B19 transgenic mice become susceptible to polyarthritis
AU - Takasawa, Naruhiko
AU - Munakata, Yasuhiko
AU - Ishii, Keiko Kumura
AU - Takahashi, Yuichi
AU - Takahashi, Minako
AU - Fu, Yi
AU - Ishii, Tomonori
AU - Fujii, Hiroshi
AU - Saito, Takako
AU - Takano, Hiroshi
AU - Noda, Tetsuo
AU - Suzuki, Misao
AU - Nose, Masato
AU - Zolla-Patzner, Suzan
AU - Sasaki, Takeshi
PY - 2004/10/1
Y1 - 2004/10/1
N2 - Human parvovirus B19 (B19) often causes acute polyarthritis in adults. In this paper, we analyzed nucleotide sequences of the B19 genome of patients with rheumatoid arthritis (RA), and then introduced the monstructual protein 1 (NS1) gene of B19 into C57BL/6 mice that had a genetic origin not susceptible to arthritis. The transgenic mice developed no lesions spontaneously, but were susceptible to type II collagen (CII)-induced arthritis. B19 NS1 was expressed in synovial cells on the articular lesions that were histologically characteristic of granulomatous synovitis and pannus formation in cartilage and bone. Serum levels of anti-CII Abs and TNF-α increased in NS1 transgenic mice to the same levels as those of DBA/1 mice, which were susceptible to polyarthritis. Stimulation with CII increased secretion of Th1-type- and Th2-type cytokines in NS1 transgenic mice, indicating that a nonpermissive H-2b haplotype in the wild type of C57BL/6 mice can be made susceptible to polyarthritis through the expression of NS1. This study is the first to show that a viral agent from the joints in humans can cause CII-induced arthritis resembling RA.
AB - Human parvovirus B19 (B19) often causes acute polyarthritis in adults. In this paper, we analyzed nucleotide sequences of the B19 genome of patients with rheumatoid arthritis (RA), and then introduced the monstructual protein 1 (NS1) gene of B19 into C57BL/6 mice that had a genetic origin not susceptible to arthritis. The transgenic mice developed no lesions spontaneously, but were susceptible to type II collagen (CII)-induced arthritis. B19 NS1 was expressed in synovial cells on the articular lesions that were histologically characteristic of granulomatous synovitis and pannus formation in cartilage and bone. Serum levels of anti-CII Abs and TNF-α increased in NS1 transgenic mice to the same levels as those of DBA/1 mice, which were susceptible to polyarthritis. Stimulation with CII increased secretion of Th1-type- and Th2-type cytokines in NS1 transgenic mice, indicating that a nonpermissive H-2b haplotype in the wild type of C57BL/6 mice can be made susceptible to polyarthritis through the expression of NS1. This study is the first to show that a viral agent from the joints in humans can cause CII-induced arthritis resembling RA.
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U2 - 10.4049/jimmunol.173.7.4675
DO - 10.4049/jimmunol.173.7.4675
M3 - Article
C2 - 15383603
AN - SCOPUS:4644285698
SN - 0022-1767
VL - 173
SP - 4675
EP - 4683
JO - Journal of Immunology
JF - Journal of Immunology
IS - 7
ER -