Akerblom L, Hinkula J, Broliden P A, Mäkitalo B, Fridberger T, Rosen J, Villacres-Eriksson M, Morein B, Wahren B
Department of Veterinary Microbiology, Faculty of Veterinary Medicine, Biomedical Center, Uppsala, Sweden.
AIDS. 1990 Oct;4(10):953-60. doi: 10.1097/00002030-199010000-00002.
Amino acid sequences inducing neutralizing antibodies to HIV-1 were sought. Murine monoclonal antibodies (MAbs) were characterized by their reactivity with the envelope precursor gp160 or the Escherichia coli recombinant DNA products pB1 and pE3 representing the carboxy- and amino-terminal halves of mature envelope gp120. Fine mapping of the MAb determinants was performed using defined 15-mer synthetic peptides spanning the entire envelope gp120 region of HIV-1. One group of MAbs recognizes epitopes (amino acids 304-323) occurring in a small region with variable and conserved amino acid sequences of gp120. These MAbs mediate neutralization of the HIV-1 strain HTLV-IIIB (HIV-1IIIB) which was used for immunization. Nine out of 11 primary HIV-1 isolates were neutralized well or moderately well. In addition, prominent serological reactivity was noted with peptide sequences of strains of various European or American origins, but not with two HIV-1 strains of African origin. The cross-reactivity contrasts with previously described type-specific reactions to other sequences of this region. The reactivity to the short conserved site GPGR with its flanking amino acids may explain the broad sequence cross-reactivity seen with our neutralizing MAbs. Two other MAbs recognize conserved epitopes (amino acids 79-103) situated in the amino-terminal region of gp120. These MAbs did not neutralize HIV-1IIIB.
人们一直在寻找能诱导产生抗HIV-1中和抗体的氨基酸序列。鼠单克隆抗体(MAb)通过其与包膜前体gp160或代表成熟包膜gp120羧基端和氨基端的大肠杆菌重组DNA产物pB1和pE3的反应性来表征。使用跨越HIV-1包膜gp120整个区域的特定15聚体合成肽对MAb决定簇进行精细定位。一组MAb识别出现在gp120可变和保守氨基酸序列的一个小区域中的表位(氨基酸304 - 323)。这些MAb介导了用于免疫的HIV-1毒株HTLV-IIIB(HIV-1IIIB)的中和作用。11株原发性HIV-1分离株中有9株被中和得很好或较好。此外,观察到与各种欧美来源毒株的肽序列有显著的血清学反应性,但与两株非洲来源的HIV-1毒株没有反应。这种交叉反应性与先前描述的对该区域其他序列的型特异性反应形成对比。对短保守位点GPGR及其侧翼氨基酸的反应性可能解释了我们的中和MAb所见的广泛序列交叉反应性。另外两种MAb识别位于gp120氨基端区域的保守表位(氨基酸79 - 103)。这些MAb不能中和HIV-1IIIB。