Saah A J, Farzadegan H, Fox R, Nishanian P, Rinaldo C R, Phair J P, Fahey J L, Lee T H, Polk B F
National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Clin Microbiol. 1987 Sep;25(9):1605-10. doi: 10.1128/jcm.25.9.1605-1610.1987.
A current concept of the serological response to human immunodeficiency virus (HIV) infection in humans is that antibodies to core antigens (p55, p24, and p15) are detectable earlier during initial stages of antibody production than antibodies against envelope antigens (gp160, gp120, and gp41). Comparative studies of Western blot (immunoblot), radioimmunoprecipitation assay (RIPA), and enzyme-linked immunosorbent assay (ELISA) during initial antibody production are limited to case reports and have not resolved the issue. Thirty of the 37 participants who are part of a prospective study had at least one specimen that was negative for anti-gp41 but had one or more other bands on Western blot. Twenty-seven of these 30 specimens were reactive for anti-gp120/160 in the RIPA. Of the same 30 specimens, kits from Bionetics identified 2 (7%), ElectroNucleonics 4 (13%), Abbott 13 (43%), Du Pont 25 (83%), and Genetic Systems 25 (83%). All participants had evidence of serological progression by Western blot, including a gp41 band, on subsequent visits; the ELISA kits of all manufacturers identified these later specimens with greater accuracy. These data show that the RIPA detects anti-envelope antibodies that may be not detectable by Western blot and that the production of anti-envelope antibodies approximately parallels the production of anti-core antibodies. The false-negative results by ELISA would permit transmission of HIV by blood transfusion from donors in early stages of infection. The sensitivity of licensed ELISA kits should be improved to identify antibody as soon as possible after infection.
目前关于人类对人类免疫缺陷病毒(HIV)感染的血清学反应的概念是,在抗体产生的初始阶段,针对核心抗原(p55、p24和p15)的抗体比针对包膜抗原(gp160、gp120和gp41)的抗体更早可检测到。在抗体产生初始阶段对蛋白质印迹法(免疫印迹法)、放射免疫沉淀测定法(RIPA)和酶联免疫吸附测定法(ELISA)的比较研究仅限于病例报告,尚未解决该问题。作为一项前瞻性研究一部分的37名参与者中,有30人至少有一份标本抗gp41呈阴性,但在蛋白质印迹法中有一条或多条其他条带。这30份标本中有27份在RIPA中抗gp120/160呈阳性。在这相同的30份标本中,Bionetics试剂盒检测出2份(7%),ElectroNucleonics检测出4份(13%),雅培检测出13份(43%),杜邦检测出25份(83%),遗传系统检测出25份(83%)。所有参与者在后续随访中通过蛋白质印迹法均有血清学进展的证据,包括出现gp41条带;所有制造商的ELISA试剂盒对这些后来的标本检测准确性更高。这些数据表明,RIPA能检测到蛋白质印迹法可能检测不到的抗包膜抗体,并且抗包膜抗体的产生大致与抗核心抗体的产生平行。ELISA出现的假阴性结果会使处于感染早期的献血者的血液传播HIV。应提高已获许可的ELISA试剂盒的灵敏度,以便在感染后尽快识别抗体。