摘要
用微量ELISA技术在包被有W6/32Terasaki微量板上,利用酶标抗人β2m抗体和抗人IgG抗体测定正常人血清或血浆,并以纯化HLAⅠ类抗原、纯化人IgG和β2m等作对照。结果显示:24份正常人血清、51份正常人血浆中HLAⅠ类抗原与IgG呈正相关,相关系数分别为r=0.9850和r=0.9696,而对照均为阴性。提示正常人血清或血浆中存在可溶性HLAⅠ类抗原IgG复合物。
On non-wettable
Terasaki trays coated with streptavidin-biotin-W6/32,24 sampl6S ofnormal serum and 51
normal plasma on the trays were determined byusing antibdies ofperoxidase-conjugated sheep
anti-β2. microglobulin and peroxidase-conjugated sheep anti-hu-man lgG, The controls
(purified HLA class I antigen, human β2 microglobulin, human IgGand 0.5%HSA-PBS)were
tested. The testing results were as follows: linear correlation ex-isted between IgG and sHLA
class I in serum of 24 healthy adults(correlation rate=0. 9850),and linear correlation between
IgG and sHLA class I in plasma of 5l healthy adults(correlation rate=0. 9696). This implicated
that soluble HLA class I antigens were presentin normal Lserum or plasma in a form of
sHLA-IgG complex. This might be the reason whysome human immunoglobulin preparations
are contaminated by soluble HLA class I anti-gen,The binding pattern and biological
significance of the complex are not yet clear , whichneed further investigation.
出处
《湖南医科大学学报》
CSCD
1995年第2期103-106,共4页
Bulletin of Hunan Medical University
基金
CBM课题
关键词
白细胞抗原
血液
β2微蛋白
免疫球蛋白G
HLA
antigen
antigen-antibody comples
soluble HLA
IgG
beta2-microglobulin
enzyme-linked
immunosorbent assaay