Serum and cervicovaginal IgG immune responses against [alpha]7 and [alpha]9 HPV in non-vaccinated women at risk for cervical cancer: Implication for catch-up prophylactic HPV vaccination

Background Cervical cancer associated with high risk-human papillomavirus (HR-HPV) infection is becoming the one of the most common female cancer in many sub-Saharan African countries. First-generation immigrant African women living in Europe are at-risk for cervical cancer, in a context of social v...

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Veröffentlicht in:PloS one 2020-05, Vol.15 (5), p.e0233084
Hauptverfasser: Prazuck, Thierry, Meye, Jean-François, Bélec, Laurent, Gubavu, Camélia, Jenabian, Mohammad-Ali, Mboumba Bouassa, Ralph-Sydney, Touzé, Antoine, Veyer, David, Péré, Hélène
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container_title PloS one
container_volume 15
creator Prazuck, Thierry
Meye, Jean-François
Bélec, Laurent
Gubavu, Camélia
Jenabian, Mohammad-Ali
Mboumba Bouassa, Ralph-Sydney
Touzé, Antoine
Veyer, David
Péré, Hélène
description Background Cervical cancer associated with high risk-human papillomavirus (HR-HPV) infection is becoming the one of the most common female cancer in many sub-Saharan African countries. First-generation immigrant African women living in Europe are at-risk for cervical cancer, in a context of social vulnerability, with frequent lack of cervical cancer screening and HPV vaccination. Objective Our objective was to address immunologically the issue of catch-up prophylactic HPV vaccination in first-generation African immigrant women living in France. Methods IgG immune responses and cross-reactivities to [alpha]7 (HPV-18, -45 and -68) and [alpha]9 (HPV-16, -31, -33, -35, -52 and -58) HPV types, including 7 HR-HPV targeted by the Gardasil-9.sup.® prophylactic vaccine, were evaluated in paired serum and cervicovaginal secretions (CVS) by HPV L1-virus-like particles-based ELISA. Genital HPV were detected by multiplex real time PCR (Seegene, Seoul, South Korea). Results Fifty-one immigrant women (mean age, 41.7 years; 72.5% HIV-infected) were prospectively included. More than two-third (68.6%) of them carried genital HPV (group I) while 31.4% were negative (group II). The majority (90.2%) exhibited serum IgG to at least one [alpha]7/[alpha]9 HR-HPV. Serum HPV-specific IgG were more frequently detected in group I than group II (100% versus 68.7%; P = 0.002). The distribution of serum and genital HPV-specific IgG was similar, but mean number of IgG reactivities to [alpha]7/[alpha]9 HR-HPV was higher in serum than CVS (5.6 IgG per woman in serum versus 3.2 in CVS; P
doi_str_mv 10.1371/journal.pone.0233084
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First-generation immigrant African women living in Europe are at-risk for cervical cancer, in a context of social vulnerability, with frequent lack of cervical cancer screening and HPV vaccination. Objective Our objective was to address immunologically the issue of catch-up prophylactic HPV vaccination in first-generation African immigrant women living in France. Methods IgG immune responses and cross-reactivities to [alpha]7 (HPV-18, -45 and -68) and [alpha]9 (HPV-16, -31, -33, -35, -52 and -58) HPV types, including 7 HR-HPV targeted by the Gardasil-9.sup.® prophylactic vaccine, were evaluated in paired serum and cervicovaginal secretions (CVS) by HPV L1-virus-like particles-based ELISA. Genital HPV were detected by multiplex real time PCR (Seegene, Seoul, South Korea). Results Fifty-one immigrant women (mean age, 41.7 years; 72.5% HIV-infected) were prospectively included. More than two-third (68.6%) of them carried genital HPV (group I) while 31.4% were negative (group II). The majority (90.2%) exhibited serum IgG to at least one [alpha]7/[alpha]9 HR-HPV. Serum HPV-specific IgG were more frequently detected in group I than group II (100% versus 68.7%; P = 0.002). The distribution of serum and genital HPV-specific IgG was similar, but mean number of IgG reactivities to [alpha]7/[alpha]9 HR-HPV was higher in serum than CVS (5.6 IgG per woman in serum versus 3.2 in CVS; P&lt;0.001). Rates of IgG cross-reactivities against HPV different from detected cervicovaginal HPV were higher in serum and CVS in group I than group II. Finally, the majority of groups I and II women (68.6% and 68.7%, respectively) exhibited serum or cervicovaginal IgG to Gardasil-9.sup.® HR-HPV, with higher mean rates in group I than group II (6.1 Gardasil-9.sup.® HR-HPV per woman versus 1.4; P&lt;0.01). One-third (31.2%) of group II women did not show any serum and genital HPV-specific IgG. Conclusions Around two-third of first-generation African immigrant women living in France showed frequent ongoing genital HPV infection and high rates of circulating and genital IgG to [alpha]7/[alpha]9 HPV, generally cross-reacting, avoiding the possibility of catch-up vaccination. Nevertheless, about one-third of women had no evidence of previous HPV infection, or showed only low levels of genital and circulating HR-HPV-specific IgG and could therefore be eligible for catch-up vaccination.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0233084</identifier><language>eng</language><publisher>Public Library of Science</publisher><subject>Analysis ; Cancer screening ; Cervical cancer ; Complications and side effects ; Demographic aspects ; Enzyme-linked immunosorbent assay ; Health aspects ; HIV ; HIV patients ; Immigrants ; Immune response ; Immunoglobulin G ; Infection ; Papillomavirus ; Papillomavirus infections ; Papillomavirus vaccines ; Patient outcomes ; Polymerase chain reaction ; Risk factors ; Time ; Vaccination</subject><ispartof>PloS one, 2020-05, Vol.15 (5), p.e0233084</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Prazuck, Thierry</creatorcontrib><creatorcontrib>Meye, Jean-François</creatorcontrib><creatorcontrib>Bélec, Laurent</creatorcontrib><creatorcontrib>Gubavu, Camélia</creatorcontrib><creatorcontrib>Jenabian, Mohammad-Ali</creatorcontrib><creatorcontrib>Mboumba Bouassa, Ralph-Sydney</creatorcontrib><creatorcontrib>Touzé, Antoine</creatorcontrib><creatorcontrib>Veyer, David</creatorcontrib><creatorcontrib>Péré, Hélène</creatorcontrib><title>Serum and cervicovaginal IgG immune responses against [alpha]7 and [alpha]9 HPV in non-vaccinated women at risk for cervical cancer: Implication for catch-up prophylactic HPV vaccination</title><title>PloS one</title><description>Background Cervical cancer associated with high risk-human papillomavirus (HR-HPV) infection is becoming the one of the most common female cancer in many sub-Saharan African countries. First-generation immigrant African women living in Europe are at-risk for cervical cancer, in a context of social vulnerability, with frequent lack of cervical cancer screening and HPV vaccination. Objective Our objective was to address immunologically the issue of catch-up prophylactic HPV vaccination in first-generation African immigrant women living in France. Methods IgG immune responses and cross-reactivities to [alpha]7 (HPV-18, -45 and -68) and [alpha]9 (HPV-16, -31, -33, -35, -52 and -58) HPV types, including 7 HR-HPV targeted by the Gardasil-9.sup.® prophylactic vaccine, were evaluated in paired serum and cervicovaginal secretions (CVS) by HPV L1-virus-like particles-based ELISA. Genital HPV were detected by multiplex real time PCR (Seegene, Seoul, South Korea). Results Fifty-one immigrant women (mean age, 41.7 years; 72.5% HIV-infected) were prospectively included. More than two-third (68.6%) of them carried genital HPV (group I) while 31.4% were negative (group II). The majority (90.2%) exhibited serum IgG to at least one [alpha]7/[alpha]9 HR-HPV. Serum HPV-specific IgG were more frequently detected in group I than group II (100% versus 68.7%; P = 0.002). The distribution of serum and genital HPV-specific IgG was similar, but mean number of IgG reactivities to [alpha]7/[alpha]9 HR-HPV was higher in serum than CVS (5.6 IgG per woman in serum versus 3.2 in CVS; P&lt;0.001). Rates of IgG cross-reactivities against HPV different from detected cervicovaginal HPV were higher in serum and CVS in group I than group II. Finally, the majority of groups I and II women (68.6% and 68.7%, respectively) exhibited serum or cervicovaginal IgG to Gardasil-9.sup.® HR-HPV, with higher mean rates in group I than group II (6.1 Gardasil-9.sup.® HR-HPV per woman versus 1.4; P&lt;0.01). One-third (31.2%) of group II women did not show any serum and genital HPV-specific IgG. Conclusions Around two-third of first-generation African immigrant women living in France showed frequent ongoing genital HPV infection and high rates of circulating and genital IgG to [alpha]7/[alpha]9 HPV, generally cross-reacting, avoiding the possibility of catch-up vaccination. Nevertheless, about one-third of women had no evidence of previous HPV infection, or showed only low levels of genital and circulating HR-HPV-specific IgG and could therefore be eligible for catch-up vaccination.</description><subject>Analysis</subject><subject>Cancer screening</subject><subject>Cervical cancer</subject><subject>Complications and side effects</subject><subject>Demographic aspects</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Health aspects</subject><subject>HIV</subject><subject>HIV patients</subject><subject>Immigrants</subject><subject>Immune response</subject><subject>Immunoglobulin G</subject><subject>Infection</subject><subject>Papillomavirus</subject><subject>Papillomavirus infections</subject><subject>Papillomavirus vaccines</subject><subject>Patient outcomes</subject><subject>Polymerase chain reaction</subject><subject>Risk factors</subject><subject>Time</subject><subject>Vaccination</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpNjl1LwzAUhoMoqNN_4EVA8K4zH23aeCei22Cg4PBGZJxmaZvZJiVpJ_41f511m7Cr88FznvcgdEXJmPKU3q5d7y3U49ZZPSaMc5LFR-iMSs4iwQg_PuhP0XkIa0ISnglxhn5ete8bDHaFlfYbo9wGSjPI8KycYNM0vdXY6zCogw4YSjA2dPgd6raCj3R7uB8knr68YWOxdTbagFKDptMr_OUabTF02JvwiQvn90lDhgI79Hd41rT1sOiMszsAOlVFfYtb79rquwbVGbXV_3sH8gKdFFAHfbmvI7R4elw8TKP582T2cD-PykQmUZzlPJEcmI6hgJgISVQhdFpImQkqChYDZDLNE0JYztKEC0bzVUETkeuYK8VH6HqnLaHWS2ML13lQjQlqeS9YzDJJaTJQNwdUpaHuquDq_u_RcAj-AtSjhn4</recordid><startdate>20200518</startdate><enddate>20200518</enddate><creator>Prazuck, Thierry</creator><creator>Meye, Jean-François</creator><creator>Bélec, Laurent</creator><creator>Gubavu, Camélia</creator><creator>Jenabian, Mohammad-Ali</creator><creator>Mboumba Bouassa, Ralph-Sydney</creator><creator>Touzé, Antoine</creator><creator>Veyer, David</creator><creator>Péré, Hélène</creator><general>Public Library of Science</general><scope/></search><sort><creationdate>20200518</creationdate><title>Serum and cervicovaginal IgG immune responses against [alpha]7 and [alpha]9 HPV in non-vaccinated women at risk for cervical cancer: Implication for catch-up prophylactic HPV vaccination</title><author>Prazuck, Thierry ; Meye, Jean-François ; Bélec, Laurent ; Gubavu, Camélia ; Jenabian, Mohammad-Ali ; Mboumba Bouassa, Ralph-Sydney ; Touzé, Antoine ; Veyer, David ; Péré, Hélène</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g595-48b3593a2e4afa40690cf6e7f998616f24aa897b5002b2753621bdf156be43cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Analysis</topic><topic>Cancer screening</topic><topic>Cervical cancer</topic><topic>Complications and side effects</topic><topic>Demographic aspects</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Health aspects</topic><topic>HIV</topic><topic>HIV patients</topic><topic>Immigrants</topic><topic>Immune response</topic><topic>Immunoglobulin G</topic><topic>Infection</topic><topic>Papillomavirus</topic><topic>Papillomavirus infections</topic><topic>Papillomavirus vaccines</topic><topic>Patient outcomes</topic><topic>Polymerase chain reaction</topic><topic>Risk factors</topic><topic>Time</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prazuck, Thierry</creatorcontrib><creatorcontrib>Meye, Jean-François</creatorcontrib><creatorcontrib>Bélec, Laurent</creatorcontrib><creatorcontrib>Gubavu, Camélia</creatorcontrib><creatorcontrib>Jenabian, Mohammad-Ali</creatorcontrib><creatorcontrib>Mboumba Bouassa, Ralph-Sydney</creatorcontrib><creatorcontrib>Touzé, Antoine</creatorcontrib><creatorcontrib>Veyer, David</creatorcontrib><creatorcontrib>Péré, Hélène</creatorcontrib><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prazuck, Thierry</au><au>Meye, Jean-François</au><au>Bélec, Laurent</au><au>Gubavu, Camélia</au><au>Jenabian, Mohammad-Ali</au><au>Mboumba Bouassa, Ralph-Sydney</au><au>Touzé, Antoine</au><au>Veyer, David</au><au>Péré, Hélène</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum and cervicovaginal IgG immune responses against [alpha]7 and [alpha]9 HPV in non-vaccinated women at risk for cervical cancer: Implication for catch-up prophylactic HPV vaccination</atitle><jtitle>PloS one</jtitle><date>2020-05-18</date><risdate>2020</risdate><volume>15</volume><issue>5</issue><spage>e0233084</spage><pages>e0233084-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Background Cervical cancer associated with high risk-human papillomavirus (HR-HPV) infection is becoming the one of the most common female cancer in many sub-Saharan African countries. First-generation immigrant African women living in Europe are at-risk for cervical cancer, in a context of social vulnerability, with frequent lack of cervical cancer screening and HPV vaccination. Objective Our objective was to address immunologically the issue of catch-up prophylactic HPV vaccination in first-generation African immigrant women living in France. Methods IgG immune responses and cross-reactivities to [alpha]7 (HPV-18, -45 and -68) and [alpha]9 (HPV-16, -31, -33, -35, -52 and -58) HPV types, including 7 HR-HPV targeted by the Gardasil-9.sup.® prophylactic vaccine, were evaluated in paired serum and cervicovaginal secretions (CVS) by HPV L1-virus-like particles-based ELISA. Genital HPV were detected by multiplex real time PCR (Seegene, Seoul, South Korea). Results Fifty-one immigrant women (mean age, 41.7 years; 72.5% HIV-infected) were prospectively included. More than two-third (68.6%) of them carried genital HPV (group I) while 31.4% were negative (group II). The majority (90.2%) exhibited serum IgG to at least one [alpha]7/[alpha]9 HR-HPV. Serum HPV-specific IgG were more frequently detected in group I than group II (100% versus 68.7%; P = 0.002). The distribution of serum and genital HPV-specific IgG was similar, but mean number of IgG reactivities to [alpha]7/[alpha]9 HR-HPV was higher in serum than CVS (5.6 IgG per woman in serum versus 3.2 in CVS; P&lt;0.001). Rates of IgG cross-reactivities against HPV different from detected cervicovaginal HPV were higher in serum and CVS in group I than group II. Finally, the majority of groups I and II women (68.6% and 68.7%, respectively) exhibited serum or cervicovaginal IgG to Gardasil-9.sup.® HR-HPV, with higher mean rates in group I than group II (6.1 Gardasil-9.sup.® HR-HPV per woman versus 1.4; P&lt;0.01). One-third (31.2%) of group II women did not show any serum and genital HPV-specific IgG. Conclusions Around two-third of first-generation African immigrant women living in France showed frequent ongoing genital HPV infection and high rates of circulating and genital IgG to [alpha]7/[alpha]9 HPV, generally cross-reacting, avoiding the possibility of catch-up vaccination. Nevertheless, about one-third of women had no evidence of previous HPV infection, or showed only low levels of genital and circulating HR-HPV-specific IgG and could therefore be eligible for catch-up vaccination.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0233084</doi></addata></record>
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subjects Analysis
Cancer screening
Cervical cancer
Complications and side effects
Demographic aspects
Enzyme-linked immunosorbent assay
Health aspects
HIV
HIV patients
Immigrants
Immune response
Immunoglobulin G
Infection
Papillomavirus
Papillomavirus infections
Papillomavirus vaccines
Patient outcomes
Polymerase chain reaction
Risk factors
Time
Vaccination
title Serum and cervicovaginal IgG immune responses against [alpha]7 and [alpha]9 HPV in non-vaccinated women at risk for cervical cancer: Implication for catch-up prophylactic HPV vaccination
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