Impairment of CD4(+) T cell responses during chronic virus infection prevents neutralizing antibody responses against virus escape mutants.

Journal article

We have shown previously that neutralizing antibodies (nAbs) are important contributors to the long-term immune control of lymphocytic choriomeningitis virus infection, particularly if cytotoxic T cell responses are low or absent. Nevertheless, virus escape from the nAb response due to mutations within the surface glycoprotein gene may subsequently allow the virus to persist. Here we show that most of the antibody-escape viral mutants retain their immunogenicity. We present evidence that the failure of the infected host to mount effective humoral responses against emerging neutralization-escape mutants correlates with the rapid loss of CD4(+) T cell responsiveness during the establishment of viral persistence. Similar mechanisms may contribute to the persistence of some human pathogens such as hepatitis B and C viruses, and human immunodeficiency virus.

Authors: Ciurea, A; Hunziker, L; Klenerman, P; Hengartner, H; Zinkernagel, R

• Publication status: Published
• Journal: Journal of experimental medicine
• Volume: 193
• Issue: 3
• Pages: 297-305
• Publication date: 2001-02-01
• DOI: 10.1084/jem.193.3.297
• EISSN: 1540-9538
• ISSN: 0022-1007
• Language: English
• Keywords: Cell Line; Cricetinae; Antigens, Viral; Glycoproteins; Lymphocytic Choriomeningitis; Humans; Mice, Transgenic; Lymphocytic choriomeningitis virus; Mice, Knockout; CD4-Positive T-Lymphocytes; Neutralization Tests; Chronic Disease; Genetic Variation; Mice; Viral Proteins; Point Mutation; Antibodies, Viral; Animals