Human papillomavirus immunization is associated with increased expression of different innate immune regulatory receptors
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Human papillomavirus (HPV) is able to inhibit the secretion of gamma interferon (IFN-γ) and the expression of some immune innate cell receptors. Immunoglobulin-like transcript 2 (ILT2) is a regulatory receptor that seems to participate in the pathogenesis of viral infections. We have studied the expression and function of ILT2 and the expression of other NK cell receptors in 23 healthy women before and after immunization with the quadrivalent HPV (type 6/11/16/18) vaccine (Gardasil). Receptor expression was analyzed by flow cytometry in freshly isolated peripheral blood mononuclear cells as well as after in vitro stimulation with the quadrivalent HPV (type 6/11/16/18) vaccine. In addition, the regulatory function of ILT2 on cell proliferation and IFN-γ production was analyzed. We found a significant increase in the expression of ILT2 by NK and CD3 CD56 lymphocytes and monocytes after quadrivalent HPV (type 6/11/16/18) vaccine immunization. In addition, the in vitro stimulation with the quadrivalent HPV (type 6/11/16/18) vaccine also increased the proportion of CD3- CD56 ILT2 NK cells. Although the inhibitory function of ILT2 on cell proliferation was enhanced after HPV immunization, the in vitro engagement of this receptor did not affect the synthesis of IFN-γ induced by HPV. Finally, a significant increase in the expression of NKG2D, NKp30, and NKp46 by NK and CD3 CD56 lymphocytes was detected after quadrivalent HPV (type 6/11/16/18) vaccine immunization. Our data indicate that HPV immunization is associated with significant changes in the expression and function of different innate immune receptors, including ILT2, which may participate in the protective effect of HPV vaccines. Copyright © 2012, American Society for Microbiology. All Rights Reserved.
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Human papillomavirus (HPV) is able to inhibit the secretion of gamma interferon (IFN-γ) and the expression of some immune innate cell receptors. Immunoglobulin-like transcript 2 (ILT2) is a regulatory receptor that seems to participate in the pathogenesis of viral infections. We have studied the expression and function of ILT2 and the expression of other NK cell receptors in 23 healthy women before and after immunization with the quadrivalent HPV (type 6/11/16/18) vaccine (Gardasil). Receptor expression was analyzed by flow cytometry in freshly isolated peripheral blood mononuclear cells as well as after in vitro stimulation with the quadrivalent HPV (type 6/11/16/18) vaccine. In addition, the regulatory function of ILT2 on cell proliferation and IFN-γ production was analyzed. We found a significant increase in the expression of ILT2 by NK and CD3%2b CD56%2b lymphocytes and monocytes after quadrivalent HPV (type 6/11/16/18) vaccine immunization. In addition, the in vitro stimulation with the quadrivalent HPV (type 6/11/16/18) vaccine also increased the proportion of CD3- CD56%2b ILT2%2b NK cells. Although the inhibitory function of ILT2 on cell proliferation was enhanced after HPV immunization, the in vitro engagement of this receptor did not affect the synthesis of IFN-γ induced by HPV. Finally, a significant increase in the expression of NKG2D, NKp30, and NKp46 by NK and CD3%2b CD56%2b lymphocytes was detected after quadrivalent HPV (type 6/11/16/18) vaccine immunization. Our data indicate that HPV immunization is associated with significant changes in the expression and function of different innate immune receptors, including ILT2, which may participate in the protective effect of HPV vaccines. Copyright © 2012, American Society for Microbiology. All Rights Reserved.
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CD3 antigen; CD56 antigen; cell receptor; gamma interferon; immunoglobulin like transcript 2 protein; natural cytotoxicity triggering receptor 1; natural cytotoxicity triggering receptor 3; natural killer cell receptor; natural killer cell receptor NKG2D; unclassified drug; Wart virus vaccine; adolescent; adult; article; CD3 T lymphocyte; cell proliferation; cytokine production; drug effect; female; flow cytometry; human; human cell; human experiment; immunization; in vitro study; innate immunity; normal human; peripheral blood mononuclear cell; priority journal; protein expression; protein function; upregulation; Wart virus; Adolescent; Adult; Antigens, CD; Cell Proliferation; Female; Flow Cytometry; Humans; Immunity, Innate; Immunophenotyping; Interferon-gamma; Killer Cells, Natural; Lymphocytes; Monocytes; Papillomavirus Vaccines; Receptors, Immunologic; Young Adult
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CD3 antigen; CD56 antigen; cell receptor; gamma interferon; immunoglobulin like transcript 2 protein; natural cytotoxicity triggering receptor 1; natural cytotoxicity triggering receptor 3; natural killer cell receptor; natural killer cell receptor NKG2D; unclassified drug; Wart virus vaccine; adolescent; adult; article; CD3+ T lymphocyte; cell proliferation; cytokine production; drug effect; female; flow cytometry; human; human cell; human experiment; immunization; in vitro study; innate immunity; normal human; peripheral blood mononuclear cell; priority journal; protein expression; protein function; upregulation; Wart virus; Adolescent; Adult; Antigens, CD; Cell Proliferation; Female; Flow Cytometry; Humans; Immunity, Innate; Immunophenotyping; Interferon-gamma; Killer Cells, Natural; Lymphocytes; Monocytes; Papillomavirus Vaccines; Receptors, Immunologic; Young Adult
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