Macaques Infected with Live Attenuated SIVmac Are Protected against Superinfection via the Rectal Mucosa

• Published in: Virology (New York, N.Y.) N.Y.), 1997-03, Vol.229 (1), p.143-154
• Main Authors: Cranage, M.P, Whatmore, A.M, Sharpe, S.A, Cook, N, Polyanskaya, N, Leech, S, Smith, J.D, Rud, E.W, Dennis, M.J, Hall, G.A
• Format: Article
• Language: English
• Subjects: AIDS/HIV; Animals; Cloning, Molecular; Genes, nef; Immunity, Mucosal; Intestinal Mucosa - immunology; Lymphoid Tissue - immunology; Macaca mulatta; Polymerase Chain Reaction; Reassortant Viruses - pathogenicity; Rectum - immunology; Sequence Deletion; simian immunodeficiency virus; Simian Immunodeficiency Virus - genetics; Simian Immunodeficiency Virus - pathogenicity; Superinfection - prevention & control; T-Lymphocytes, Cytotoxic - immunology; Vaccines, Attenuated - administration & dosage; Vaccines, Attenuated - immunology; Viral Vaccines - administration & dosage; Viral Vaccines - immunology
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1006/viro.1996.8419

Good protection against systemic challenge in the SIVmac model of AIDS has been provided by prior infection with attenuated virus. To determine if such protection extends to intrarectal mucosal challenge two molecular clones, SIVmacC8 and SIVmacJ5, were used in this study. SIVmacC8 has an attenuated phenotypein vivo,due to a 12-bp deletion in the nef/3′-LTR, whereas SIVmacJ5 has a full size nef open reading frame and induces AIDS in infected macaques. The J5 molecular clone was shown to infect rhesus macaques following atraumatic intrarectal inoculation. The dynamics were similar to those following intravenous inoculation resulting in early, high, cell-associated viremia and seroconversion. Four macaques previously infected with the attenuated SIVmacC8 resisted superinfection with SIVmacJ5, following intrarectal inoculation. These animals also resisted intrarectal infection with an HIV/SIV chimeric virus (SHIV) composed of SIVmac239 expressing the HXBc2env, tat,andrevgenes, suggesting that immunity to the envelope proteins was unlikely to be involved in the superinfection resistance. Infection with the attenuated SIVmac generated cytotoxic T lymphocytes (CTL) detectable in the peripheral circulation, serum neutralizing antibodies, and SIV-binding antibodies in rectal fluids. SIVmacC8 proviral DNA was found in lymph nodes removed at necropsy but there was no evidence for local sequestration of challenge virus. SIV-specific CTL were detected in gut-associated lymph nodes and may have a role in limiting superinfection following mucosal exposure.