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.
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 -