[HTML][HTML] GM-CSF DNA: an adjuvant for higher avidity IgG, rectal IgA, and increased protection against the acute phase of a SHIV-89.6 P challenge by a DNA/MVA …

L Lai, D Vödrös, PA Kozlowski, DC Montefiori… - Virology, 2007 - Elsevier
L Lai, D Vödrös, PA Kozlowski, DC Montefiori, RL Wilson, VL Akerstrom, L Chennareddi…
Virology, 2007Elsevier
Single intradermal or intramuscular inoculations of GM-CSF DNA with the DNA prime for a
simian–human immunodeficiency virus (SHIV)-89.6 vaccine, which consists of DNA priming
followed by modified vaccinia Ankara (MVA) boosting, increased protection of both the blood
and intestines against the acute phase of an intrarectal SHIV-89.6 P challenge. GM-CSF
appeared to contribute to protection by enhancing two antibody responses: the avidity
maturation of anti-Env IgG in blood (p=< 0.01) and the presence of long lasting anti-viral IgA …
Single intradermal or intramuscular inoculations of GM-CSF DNA with the DNA prime for a simian–human immunodeficiency virus (SHIV)-89.6 vaccine, which consists of DNA priming followed by modified vaccinia Ankara (MVA) boosting, increased protection of both the blood and intestines against the acute phase of an intrarectal SHIV-89.6P challenge. GM-CSF appeared to contribute to protection by enhancing two antibody responses: the avidity maturation of anti-Env IgG in blood (p=<0.01) and the presence of long lasting anti-viral IgA in rectal secretions (p<0.01). The avidity of anti-Env IgG showed strong correlations with protection both pre and post challenge. Animals with the highest avidity anti-Env Ab had 1000-fold reductions in peak viremia over those with the lowest avidity anti-Env Ab. The enhanced IgA response was associated with the best protection, but did not achieve significance.
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