Relationship of leukocyte CR1 transcript and protein with the pathophysiology and prognosis of systemic lupus erythematosus: A follow-up study

被引:5
作者
Arora, V. [2 ]
Grover, R. [3 ]
Kumar, A. [4 ]
Anand, D. [1 ]
Das, N. [1 ]
机构
[1] All India Inst Med Sci, Dept Biochem, New Delhi 110029, India
[2] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[3] Fortis Healthcare Ltd, Dept Nephrol, New Delhi, India
[4] Fortis Healthcare Ltd, Dept Rheumatol, New Delhi, India
关键词
complement receptor 1; follow-up; SLE disease activity index; systemic lupus erythematosus; DISEASE-ACTIVITY; RECEPTOR CR-1; REVISED CRITERIA; IMMUNE-COMPLEXES; C3B RECEPTORS; SERUM-LEVELS; COMPLEMENT; EXPRESSION; ERYTHROCYTES; LYMPHOCYTES;
D O I
10.1177/0961203311400112
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Complement Receptor 1 (CR1) is a key complement regulatory protein (CRP) involved in the clearance of immune complexes. Earlier, we reported a marked decline of leukocyte CR1 (L-CR1) transcript and protein in patients with active systemic lupus erythematosus (SLE) and suggested L-CR1 transcript as a putative non-invasive disease marker for SLE. This follow-up study involving 18 patients with active SLE was conducted for further confirmation of the relationship between L-CR1 and SLE. Blood samples from the patients were collected on day 1 of the diagnosis (0 month) and at different time intervals (3 and 6 months) for analysis of L-CR1 transcript and L-CR1 protein by semi-quantitative reverse-transcriptase-polymerase chain reaction (RT-PCR) and western blotting respectively. Within 6 months, 15 patients entered remission. On day 1, the mean values of L-CR1 transcript (8.42 +/- 3.53) and L-CR1 protein (4683 +/- 1094) in the SLE patients were 6 times and 12 times lower than the normal controls (n = 103). At the end of month 6, these values increased by 4.5 and 6.5 times respectively for CR1 transcript (37.86 +/- 8.52) and protein (30,265 +/- 8614). Simultaneously, the SLE Disease Activity Index (SLEDAI) scores decreased by 4.8 times (4.47 +/- 3.32) as compared with the scores obtained on day 1 (21.45 +/- 5.67). Moreover, CR1 values correlated negatively with the SLEDAI scores. Levels of L-CR1 protein and transcript remained low in the three patients who did not enter remission. All of the above results suggested that an increase in the levels of L-CR1 related to good prognosis. Since the levels of L-CR1 protein is influenced by variables like proteolytic cleavage and secretion from leukocytes, the values of L-CR1 transcript on day 1 and subsequent follow-up points may bring a better insight into the state of the disease activity. An extended follow-up study is needed to confirm the significance of L-CR1 as a prognostic marker for SLE. Lupus (2011) 20, 1010-1018.
引用
收藏
页码:1010 / 1018
页数:9
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