Autoantibodies against the envelope proteins of endogenous retroviruses K102 and K108 in patients with systemic lupus erythematosus correlate with active disease.
Autoantibodies against the envelope proteins of endogenous retroviruses K102 and K108 in patients with systemic lupus erythematosus correlate with active disease.
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系统性红斑狼疮患者体内抗内源性逆转录病毒K102和K108包膜蛋白的自身抗体与活动性疾病相关
DOI:
10.55563/clinexprheumatol/2kg1d8
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发表时间:
2022-07
影响因子:
3.7
通讯作者:
Mustelin T
中科院分区:
文献类型:
--
作者:
Khadjinova AI;Wang X;Laine A;Ukadike K;Eckert M;Stevens A;Bengtsson AA;Lood C;Mustelin T
To determine if patients with systemic lupus erythematosus (SLE), a disease characterised by elevated type I interferons reminiscent of anti-viral immunity, have expression of human endogenous retrovirus K (HERV-K) proviruses capable of producing envelope (Env) protein, as well as associated autoantibodies against the Env protein. ELISAs were conducted with recombinant Env protein and sera from SLE patients with active (n=60) or inactive (n=49) disease, healthy controls (n=47), other rheumatic disorders (n=59), as well as plasma from paediatric lupus patients with active (n=30) or inactive (n=30) disease, and 17 healthy children. Antibody reactivity was evaluated for correlations with clinical and laboratory parameters of the patients. Expression of HERV-K transcripts were profiled in SLE leukocytes by RNA-Seq. Both adult and paediatric SLE patients had autoantibodies against HERV-K Env with higher titers than healthy controls or patients with Sjögren’s syndrome, small- or large-vessel vasculitis, or psoriatic arthritis. Transcripts from only two HERV-K loci capable of producing Env, HERV-K102 and -K108, were detected among the 10 expressed loci in SLE patients. Our data reveal that HERV-K proviruses are expressed in SLE and that the HERV-K-encoded Env protein elicits an immune response in patients, particularly during active disease.
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影响因子:
4.4
作者:
Baudino, Lucie;Yoshinobu, Kumiko;Morito, Naoki;Kikuchi, Shuichi;Fossati-Jimack, Liliane;Morley, Bernard J.;Vyse, Timothy J.;Hirose, Sachiko;Jorgensen, Trine N.;Tucker, Rebecca M.;Roark, Christina L.;Kotzin, Brian L.;Evans, Leonard H.;Izui, Shozo
通讯作者:
Izui, Shozo
影响因子:
3.3
作者:
de Mulder M;SenGupta D;Deeks SG;Martin JN;Pilcher CD;Hecht FM;Sacha JB;Nixon DF;Michaud HA
通讯作者:
Michaud HA
影响因子:
5.4
作者:
Bhardwaj, Neeru;Maldarelli, Frank;Coffin, John M.
通讯作者:
Coffin, John M.
影响因子:
--
作者:
BLOMBERG, J;NIVED, O;STURFELT, G
通讯作者:
STURFELT, G
影响因子:
7.3
作者:
Mustelin T;Ukadike KC
通讯作者:
Ukadike KC