Immune responsiveness to the immunodominant recombinant envelope epitopes of human T lymphotropic virus types I and II in diverse geographic populations

J Infect Dis. 1992 Nov;166(5):1160-3. doi: 10.1093/infdis/166.5.1160.

Abstract

The heterogeneity of immune responsiveness to the immunodominant epitopes of human T lymphotropic virus (HTLV) types I (MTA-1(162-209)) and II (K-55(162-205)) were determined in natural infections with HTLV-I and -II from diverse geographic areas (n = 285). Of the HTLV-I specimens confirmed by polymerase chain reaction (PCR), all North American (n = 37) and Peruvian (n = 19) specimens reacted with MTA-1. Of HTLV-II specimens confirmed by PCR, 44 (96%) of 46 from North American blood donors, 28 (97%) of 29 from native Americans, and all from intravenous drug users (n = 29) reacted with K-55. Specimens from other geographic areas (Peru, 30; Brazil, 4; Mexico, 10; Italy, 5; Somalia, 13; Ethiopia, 17; Japan, 32; and Jamaica, 15) all reacted either with MTA-1 or K-55. By synthetic peptide-based serologic typing, all of these specimens could be typed as HTLV-I or -II. In addition to the direct implications of these findings for diagnostic purposes, these data provide indirect evidence for the conservation of immunodominant HTLVenv epitopes in diverse geographic populations.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Africa
  • Blood Donors
  • Epitopes / analysis*
  • Gene Products, gag / analysis*
  • Gene Products, gag / immunology*
  • Geography
  • HTLV-I Antibodies / blood*
  • HTLV-II Antibodies / blood*
  • Human T-lymphotropic virus 1 / immunology*
  • Human T-lymphotropic virus 2 / immunology*
  • Humans
  • Immunoassay
  • Jamaica
  • Mexico
  • North America
  • Polymerase Chain Reaction / methods
  • Recombinant Proteins / immunology
  • South America
  • Viral Envelope Proteins / analysis*
  • Viral Envelope Proteins / immunology*

Substances

  • Epitopes
  • Gene Products, gag
  • HTLV-I Antibodies
  • HTLV-II Antibodies
  • Recombinant Proteins
  • Viral Envelope Proteins