Immune response to pneumococcal polysaccharide vaccine in adults with chronic plaque psoriasis treated with alefacept

Background Alefacept is a T cell–modulating biologic therapy for psoriasis that could affect patients' ability to mount immune responses. Objective This open-label, phase IV, multicenter study assessed the ability of adults with chronic plaque psoriasis receiving alefacept to generate antibodie...

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Veröffentlicht in:Journal of the American Academy of Dermatology 2011-10, Vol.65 (4), p.799-806
Hauptverfasser: Lynde, Charles, MD, Krell, James, MD, Korman, Neil, MD, PhD, Mathes, Barbara, MD
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container_issue 4
container_start_page 799
container_title Journal of the American Academy of Dermatology
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creator Lynde, Charles, MD
Krell, James, MD
Korman, Neil, MD, PhD
Mathes, Barbara, MD
description Background Alefacept is a T cell–modulating biologic therapy for psoriasis that could affect patients' ability to mount immune responses. Objective This open-label, phase IV, multicenter study assessed the ability of adults with chronic plaque psoriasis receiving alefacept to generate antibodies to a pneumococcal polysaccharide vaccine (PPV). Methods Patients were treated with a standard 12-week course of alefacept and administered the 23-valent PPV at week 6. Antipneumococcal antibodies were measured at baseline and weeks 6, 9, 12, and 33. The primary end point was the percentage of patients with a 2-fold or greater increase from prevaccination (week 6) to 6 weeks postvaccination (week 12) in antibody titers to 2 or more of 5 designated PPV antigens. Results Of 43 patients enrolled, 42 were included in the full analysis set, with 86% of patients exhibiting a 2-fold or greater increase and 57% of patients exhibiting a 4-fold or greater increase in antibody titers to 2 or more of 5 designated antigens from prevaccination to 6 weeks postvaccination. At 6 months postvaccination, 78% of patients had a 2-fold or greater increase and 47% of patients had a 4-fold or greater increase in antibody titers to 2 or more of the 5 designated antigens. There were statistically significant increases in mean antibody titers to all 23 antigens in PPV from prevaccination to 6 weeks postvaccination. Limitations This was an open-label study with no comparator. Conclusions Most patients mounted immune responses to PPV; increases in antibody titers in these patients were consistent with those seen in healthy individuals.
doi_str_mv 10.1016/j.jaad.2010.04.040
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Objective This open-label, phase IV, multicenter study assessed the ability of adults with chronic plaque psoriasis receiving alefacept to generate antibodies to a pneumococcal polysaccharide vaccine (PPV). Methods Patients were treated with a standard 12-week course of alefacept and administered the 23-valent PPV at week 6. Antipneumococcal antibodies were measured at baseline and weeks 6, 9, 12, and 33. The primary end point was the percentage of patients with a 2-fold or greater increase from prevaccination (week 6) to 6 weeks postvaccination (week 12) in antibody titers to 2 or more of 5 designated PPV antigens. Results Of 43 patients enrolled, 42 were included in the full analysis set, with 86% of patients exhibiting a 2-fold or greater increase and 57% of patients exhibiting a 4-fold or greater increase in antibody titers to 2 or more of 5 designated antigens from prevaccination to 6 weeks postvaccination. At 6 months postvaccination, 78% of patients had a 2-fold or greater increase and 47% of patients had a 4-fold or greater increase in antibody titers to 2 or more of the 5 designated antigens. There were statistically significant increases in mean antibody titers to all 23 antigens in PPV from prevaccination to 6 weeks postvaccination. Limitations This was an open-label study with no comparator. Conclusions Most patients mounted immune responses to PPV; increases in antibody titers in these patients were consistent with those seen in healthy individuals.</description><identifier>ISSN: 0190-9622</identifier><identifier>EISSN: 1097-6787</identifier><identifier>DOI: 10.1016/j.jaad.2010.04.040</identifier><identifier>PMID: 21453987</identifier><identifier>CODEN: JAADDB</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; alefacept ; Bacterial diseases ; Biological and medical sciences ; biologics ; Dermatology ; Human bacterial diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Middle Aged ; pneumococcal polysaccharide vaccine ; Pneumococcal Vaccines - immunology ; Prevention and actions ; psoriasis ; Psoriasis - drug therapy ; Psoriasis - immunology ; Psoriasis. Parapsoriasis. Lichen ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Recombinant Fusion Proteins - therapeutic use ; Staphylococcal infections, streptococcal infections, pneumococcal infections ; T cells ; vaccines</subject><ispartof>Journal of the American Academy of Dermatology, 2011-10, Vol.65 (4), p.799-806</ispartof><rights>American Academy of Dermatology, Inc.</rights><rights>2010 American Academy of Dermatology, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 American Academy of Dermatology, Inc. Published by Mosby, Inc. 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Objective This open-label, phase IV, multicenter study assessed the ability of adults with chronic plaque psoriasis receiving alefacept to generate antibodies to a pneumococcal polysaccharide vaccine (PPV). Methods Patients were treated with a standard 12-week course of alefacept and administered the 23-valent PPV at week 6. Antipneumococcal antibodies were measured at baseline and weeks 6, 9, 12, and 33. The primary end point was the percentage of patients with a 2-fold or greater increase from prevaccination (week 6) to 6 weeks postvaccination (week 12) in antibody titers to 2 or more of 5 designated PPV antigens. Results Of 43 patients enrolled, 42 were included in the full analysis set, with 86% of patients exhibiting a 2-fold or greater increase and 57% of patients exhibiting a 4-fold or greater increase in antibody titers to 2 or more of 5 designated antigens from prevaccination to 6 weeks postvaccination. At 6 months postvaccination, 78% of patients had a 2-fold or greater increase and 47% of patients had a 4-fold or greater increase in antibody titers to 2 or more of the 5 designated antigens. There were statistically significant increases in mean antibody titers to all 23 antigens in PPV from prevaccination to 6 weeks postvaccination. Limitations This was an open-label study with no comparator. Conclusions Most patients mounted immune responses to PPV; increases in antibody titers in these patients were consistent with those seen in healthy individuals.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>alefacept</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>biologics</subject><subject>Dermatology</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>pneumococcal polysaccharide vaccine</subject><subject>Pneumococcal Vaccines - immunology</subject><subject>Prevention and actions</subject><subject>psoriasis</subject><subject>Psoriasis - drug therapy</subject><subject>Psoriasis - immunology</subject><subject>Psoriasis. Parapsoriasis. Lichen</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Staphylococcal infections, streptococcal infections, pneumococcal infections</subject><subject>T cells</subject><subject>vaccines</subject><issn>0190-9622</issn><issn>1097-6787</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ks-r1DAQgIMovvXpP-BBchFPXZM0bRoQQR7-ePDAg3oO02TKZk2bmrRP9r83ZVcFD8JAQvhmmPkyhDznbM8Zb18f90cAtxesPDBZgj0gO860qlrVqYdkx7hmlW6FuCJPcj4yxrSs1WNyJbhsat2pHVlvx3GdkCbMc5wy0iXSecJ1jDZaC4HOMZwyWHuA5B3S-3L1hfcTBbeGJdOffjlQe0hx8pbOAX6sSOcck4fsM10SwoLuTEHAASzOy1PyaICQ8dnlvCbfPrz_evOpuvv88fbm3V1lpWRLZXnDJAy9Usr1snaNbmunlWIwaN70gxWy49D2wrWCa1Vbi05D17PGdkqour4mr8515xRLX3kxo88WQ4AJ45pNp1nbcSFEIcWZtCnmnHAwc_IjpJPhzGy2zdFsts1m2zBZgpWkF5fyaz-i-5PyW28BXl4AyEXmkGCyPv_lZKOE5hv35sxhkXHvMZlsPU5lHJ_QLsZF__8-3v6TboMv3wHhO54wH-OapqLZcJOFYebLthfbWvCyEQ1v6voXKfu0VQ</recordid><startdate>20111001</startdate><enddate>20111001</enddate><creator>Lynde, Charles, MD</creator><creator>Krell, James, MD</creator><creator>Korman, Neil, MD, PhD</creator><creator>Mathes, Barbara, MD</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20111001</creationdate><title>Immune response to pneumococcal polysaccharide vaccine in adults with chronic plaque psoriasis treated with alefacept</title><author>Lynde, Charles, MD ; Krell, James, MD ; Korman, Neil, MD, PhD ; Mathes, Barbara, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-c1504afb777db43d5963d9770af915bfc2481a6b2d621973cced9a8b05c872733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>alefacept</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>biologics</topic><topic>Dermatology</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>pneumococcal polysaccharide vaccine</topic><topic>Pneumococcal Vaccines - immunology</topic><topic>Prevention and actions</topic><topic>psoriasis</topic><topic>Psoriasis - drug therapy</topic><topic>Psoriasis - immunology</topic><topic>Psoriasis. Parapsoriasis. Lichen</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>Staphylococcal infections, streptococcal infections, pneumococcal infections</topic><topic>T cells</topic><topic>vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynde, Charles, MD</creatorcontrib><creatorcontrib>Krell, James, MD</creatorcontrib><creatorcontrib>Korman, Neil, MD, PhD</creatorcontrib><creatorcontrib>Mathes, Barbara, MD</creatorcontrib><creatorcontrib>Vaccine Study Investigators</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Academy of Dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynde, Charles, MD</au><au>Krell, James, MD</au><au>Korman, Neil, MD, PhD</au><au>Mathes, Barbara, MD</au><aucorp>Vaccine Study Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune response to pneumococcal polysaccharide vaccine in adults with chronic plaque psoriasis treated with alefacept</atitle><jtitle>Journal of the American Academy of Dermatology</jtitle><addtitle>J Am Acad Dermatol</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>65</volume><issue>4</issue><spage>799</spage><epage>806</epage><pages>799-806</pages><issn>0190-9622</issn><eissn>1097-6787</eissn><coden>JAADDB</coden><abstract>Background Alefacept is a T cell–modulating biologic therapy for psoriasis that could affect patients' ability to mount immune responses. Objective This open-label, phase IV, multicenter study assessed the ability of adults with chronic plaque psoriasis receiving alefacept to generate antibodies to a pneumococcal polysaccharide vaccine (PPV). Methods Patients were treated with a standard 12-week course of alefacept and administered the 23-valent PPV at week 6. Antipneumococcal antibodies were measured at baseline and weeks 6, 9, 12, and 33. The primary end point was the percentage of patients with a 2-fold or greater increase from prevaccination (week 6) to 6 weeks postvaccination (week 12) in antibody titers to 2 or more of 5 designated PPV antigens. Results Of 43 patients enrolled, 42 were included in the full analysis set, with 86% of patients exhibiting a 2-fold or greater increase and 57% of patients exhibiting a 4-fold or greater increase in antibody titers to 2 or more of 5 designated antigens from prevaccination to 6 weeks postvaccination. At 6 months postvaccination, 78% of patients had a 2-fold or greater increase and 47% of patients had a 4-fold or greater increase in antibody titers to 2 or more of the 5 designated antigens. There were statistically significant increases in mean antibody titers to all 23 antigens in PPV from prevaccination to 6 weeks postvaccination. Limitations This was an open-label study with no comparator. Conclusions Most patients mounted immune responses to PPV; increases in antibody titers in these patients were consistent with those seen in healthy individuals.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>21453987</pmid><doi>10.1016/j.jaad.2010.04.040</doi><tpages>8</tpages></addata></record>
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subjects Adolescent
Adult
Aged
alefacept
Bacterial diseases
Biological and medical sciences
biologics
Dermatology
Human bacterial diseases
Humans
Infectious diseases
Male
Medical sciences
Middle Aged
pneumococcal polysaccharide vaccine
Pneumococcal Vaccines - immunology
Prevention and actions
psoriasis
Psoriasis - drug therapy
Psoriasis - immunology
Psoriasis. Parapsoriasis. Lichen
Public health. Hygiene
Public health. Hygiene-occupational medicine
Recombinant Fusion Proteins - therapeutic use
Staphylococcal infections, streptococcal infections, pneumococcal infections
T cells
vaccines
title Immune response to pneumococcal polysaccharide vaccine in adults with chronic plaque psoriasis treated with alefacept
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