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Adoptive immunotherapy of feline immunodeficiency virus with autologous ex vivo-stimulated lymphoid cells modulates virus and T-cell subsets in blood.
Clin Diagn Lab Immunol. 2005 Jun; 12(6):736-45.CD

Abstract

The potential of immunotherapy with autologous virus-specific T cells to affect the course of feline immunodeficiency virus (FIV) infection was explored in a group of specific-pathogen-free cats infected with FIV a minimum of 10 months earlier. Popliteal lymph node cells were stimulated by cocultivation with UV-inactivated autologous fibroblasts infected with recombinant vaccinia viruses expressing either FIV gag or env gene products, followed by expansion in interleukin-2. One or two infusions of both Gag- and Env-stimulated cells resulted in a slow increase in FIV-specific gamma interferon-secreting T cells in the circulation of cats. In the same animals, viral set points fluctuated widely during the first 2 to 3 weeks after adoptive transfer and then returned to pretreatment levels. The preexisting viral quasispecies was also found to be modulated, whereas no novel viral variants were detected. Circulating CD4(+) counts underwent a dramatic decline early after treatment. CD4/CD8 ratios remained instead essentially unchanged and eventually improved in some animals. In contrast, a single infusion of Gag-stimulated cells alone produced no apparent modulations of infection.

Authors+Show Affiliations

Dipartimento di Patologia Sperimentale, Università di Pisa, Via San Zeno 37, I-56127 Pisa, Italy.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

15939748

Citation

Flynn, J Norman, et al. "Adoptive Immunotherapy of Feline Immunodeficiency Virus With Autologous Ex Vivo-stimulated Lymphoid Cells Modulates Virus and T-cell Subsets in Blood." Clinical and Diagnostic Laboratory Immunology, vol. 12, no. 6, 2005, pp. 736-45.
Flynn JN, Pistello M, Isola P, et al. Adoptive immunotherapy of feline immunodeficiency virus with autologous ex vivo-stimulated lymphoid cells modulates virus and T-cell subsets in blood. Clin Diagn Lab Immunol. 2005;12(6):736-45.
Flynn, J. N., Pistello, M., Isola, P., Zaccaro, L., Del Santo, B., Ricci, E., Matteucci, D., & Bendinelli, M. (2005). Adoptive immunotherapy of feline immunodeficiency virus with autologous ex vivo-stimulated lymphoid cells modulates virus and T-cell subsets in blood. Clinical and Diagnostic Laboratory Immunology, 12(6), 736-45.
Flynn JN, et al. Adoptive Immunotherapy of Feline Immunodeficiency Virus With Autologous Ex Vivo-stimulated Lymphoid Cells Modulates Virus and T-cell Subsets in Blood. Clin Diagn Lab Immunol. 2005;12(6):736-45. PubMed PMID: 15939748.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Adoptive immunotherapy of feline immunodeficiency virus with autologous ex vivo-stimulated lymphoid cells modulates virus and T-cell subsets in blood. AU - Flynn,J Norman, AU - Pistello,Mauro, AU - Isola,Patrizia, AU - Zaccaro,Lucia, AU - Del Santo,Barbara, AU - Ricci,Enrica, AU - Matteucci,Donatella, AU - Bendinelli,Mauro, PY - 2005/6/9/pubmed PY - 2006/4/13/medline PY - 2005/6/9/entrez SP - 736 EP - 45 JF - Clinical and diagnostic laboratory immunology JO - Clin Diagn Lab Immunol VL - 12 IS - 6 N2 - The potential of immunotherapy with autologous virus-specific T cells to affect the course of feline immunodeficiency virus (FIV) infection was explored in a group of specific-pathogen-free cats infected with FIV a minimum of 10 months earlier. Popliteal lymph node cells were stimulated by cocultivation with UV-inactivated autologous fibroblasts infected with recombinant vaccinia viruses expressing either FIV gag or env gene products, followed by expansion in interleukin-2. One or two infusions of both Gag- and Env-stimulated cells resulted in a slow increase in FIV-specific gamma interferon-secreting T cells in the circulation of cats. In the same animals, viral set points fluctuated widely during the first 2 to 3 weeks after adoptive transfer and then returned to pretreatment levels. The preexisting viral quasispecies was also found to be modulated, whereas no novel viral variants were detected. Circulating CD4(+) counts underwent a dramatic decline early after treatment. CD4/CD8 ratios remained instead essentially unchanged and eventually improved in some animals. In contrast, a single infusion of Gag-stimulated cells alone produced no apparent modulations of infection. SN - 1071-412X UR - https://www.unboundmedicine.com/medline/citation/15939748/Adoptive_immunotherapy_of_feline_immunodeficiency_virus_with_autologous_ex_vivo_stimulated_lymphoid_cells_modulates_virus_and_T_cell_subsets_in_blood_ DB - PRIME DP - Unbound Medicine ER -