Localization of T and B cell stimulating domains of the immunodominant 33-kDa protein of Onchocerca volvulus (Ov33)
The localization of T and B cell epitopes on a well characterized 33-kDa protein of the filarial nematode Onchocerca volvulus (Ov33) was studied using peripheral blood mononuclear cells (PBMC) and sera from a total of 52 onchocerciasis patients with the generalized form of infection. A proportion of...
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Veröffentlicht in: | Clinical immunology and immunopathology 1997-10, Vol.85 (1), p.56-66 |
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description | The localization of T and B cell epitopes on a well characterized 33-kDa protein of the filarial nematode Onchocerca volvulus (Ov33) was studied using peripheral blood mononuclear cells (PBMC) and sera from a total of 52 onchocerciasis patients with the generalized form of infection. A proportion of the PBMC samples proliferated in response to recombinant Ov33-GST fusion protein and to fusion free Ov33-6xHis. Proliferative responses of patient PBMC to seven truncated Ov33-6xHis polypeptides and to three synthetic peptides revealed at least one major and two minor T cell epitopes in the protein. The dominant T cell stimulating domain was localized between amino acids 113 and 143. ELISA studies with the Ov33-GST fusion protein revealed that patient sera contained Ov33-specific IgG1, IgG4, IgE, and IgM antibodies. Analysis of the IgG4 response with 10 truncated Ov33 polypeptides identified four B cell stimulating domains in the N-terminal, central, and C-terminal region of the molecule. The B cell domain recognized by the majority of sera was localized between amino acids 113 and 143. The data indicate that this region of the protein is the major T and B cell stimulating domain of Ov33 and might be relevant for vaccine development and for improved immunodiagnosis of onchocerciasis. |
doi_str_mv | 10.1006/clin.1997.4400 |
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N ; ADAM, R ; SEEBER, F ; ZIPFEL, P. F ; TITANJI, V. P. K ; LUCIUS, R</creator><creatorcontrib>POGONKA, T ; BRATTIG, N ; NDE, P. N ; ADAM, R ; SEEBER, F ; ZIPFEL, P. F ; TITANJI, V. P. K ; LUCIUS, R</creatorcontrib><description>The localization of T and B cell epitopes on a well characterized 33-kDa protein of the filarial nematode Onchocerca volvulus (Ov33) was studied using peripheral blood mononuclear cells (PBMC) and sera from a total of 52 onchocerciasis patients with the generalized form of infection. A proportion of the PBMC samples proliferated in response to recombinant Ov33-GST fusion protein and to fusion free Ov33-6xHis. Proliferative responses of patient PBMC to seven truncated Ov33-6xHis polypeptides and to three synthetic peptides revealed at least one major and two minor T cell epitopes in the protein. The dominant T cell stimulating domain was localized between amino acids 113 and 143. ELISA studies with the Ov33-GST fusion protein revealed that patient sera contained Ov33-specific IgG1, IgG4, IgE, and IgM antibodies. Analysis of the IgG4 response with 10 truncated Ov33 polypeptides identified four B cell stimulating domains in the N-terminal, central, and C-terminal region of the molecule. The B cell domain recognized by the majority of sera was localized between amino acids 113 and 143. The data indicate that this region of the protein is the major T and B cell stimulating domain of Ov33 and might be relevant for vaccine development and for improved immunodiagnosis of onchocerciasis.</description><identifier>ISSN: 0090-1229</identifier><identifier>EISSN: 1090-2341</identifier><identifier>DOI: 10.1006/clin.1997.4400</identifier><identifier>PMID: 9325070</identifier><identifier>CODEN: CLIIAT</identifier><language>eng</language><publisher>San Diego, CA: Academic Press</publisher><subject>Adolescent ; Adult ; Aged ; Amino Acid Sequence ; Animals ; Antibodies, Helminth - blood ; Antigens, Helminth - chemistry ; Antigens, Helminth - genetics ; B-Lymphocytes - immunology ; Biological and medical sciences ; Diseases caused by nematodes ; Female ; Filariases ; Helminth Proteins - chemistry ; Helminth Proteins - genetics ; Helminth Proteins - immunology ; Helminthic diseases ; Humans ; Immunodominant Epitopes - chemistry ; Immunodominant Epitopes - genetics ; In Vitro Techniques ; Infectious diseases ; Lymphocyte Activation ; Male ; Medical sciences ; Middle Aged ; Molecular Sequence Data ; Molecular Weight ; Onchocerca volvulus - genetics ; Onchocerca volvulus - immunology ; Onchocerciasis - immunology ; Onchocercosis ; Parasitic diseases ; Recombinant Fusion Proteins - chemistry ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - immunology ; T-Lymphocytes - immunology</subject><ispartof>Clinical immunology and immunopathology, 1997-10, Vol.85 (1), p.56-66</ispartof><rights>1997 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2857922$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9325070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>POGONKA, T</creatorcontrib><creatorcontrib>BRATTIG, N</creatorcontrib><creatorcontrib>NDE, P. N</creatorcontrib><creatorcontrib>ADAM, R</creatorcontrib><creatorcontrib>SEEBER, F</creatorcontrib><creatorcontrib>ZIPFEL, P. F</creatorcontrib><creatorcontrib>TITANJI, V. P. K</creatorcontrib><creatorcontrib>LUCIUS, R</creatorcontrib><title>Localization of T and B cell stimulating domains of the immunodominant 33-kDa protein of Onchocerca volvulus (Ov33)</title><title>Clinical immunology and immunopathology</title><addtitle>Clin Immunol Immunopathol</addtitle><description>The localization of T and B cell epitopes on a well characterized 33-kDa protein of the filarial nematode Onchocerca volvulus (Ov33) was studied using peripheral blood mononuclear cells (PBMC) and sera from a total of 52 onchocerciasis patients with the generalized form of infection. A proportion of the PBMC samples proliferated in response to recombinant Ov33-GST fusion protein and to fusion free Ov33-6xHis. Proliferative responses of patient PBMC to seven truncated Ov33-6xHis polypeptides and to three synthetic peptides revealed at least one major and two minor T cell epitopes in the protein. The dominant T cell stimulating domain was localized between amino acids 113 and 143. ELISA studies with the Ov33-GST fusion protein revealed that patient sera contained Ov33-specific IgG1, IgG4, IgE, and IgM antibodies. Analysis of the IgG4 response with 10 truncated Ov33 polypeptides identified four B cell stimulating domains in the N-terminal, central, and C-terminal region of the molecule. The B cell domain recognized by the majority of sera was localized between amino acids 113 and 143. The data indicate that this region of the protein is the major T and B cell stimulating domain of Ov33 and might be relevant for vaccine development and for improved immunodiagnosis of onchocerciasis.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies, Helminth - blood</subject><subject>Antigens, Helminth - chemistry</subject><subject>Antigens, Helminth - genetics</subject><subject>B-Lymphocytes - immunology</subject><subject>Biological and medical sciences</subject><subject>Diseases caused by nematodes</subject><subject>Female</subject><subject>Filariases</subject><subject>Helminth Proteins - chemistry</subject><subject>Helminth Proteins - genetics</subject><subject>Helminth Proteins - immunology</subject><subject>Helminthic diseases</subject><subject>Humans</subject><subject>Immunodominant Epitopes - chemistry</subject><subject>Immunodominant Epitopes - genetics</subject><subject>In Vitro Techniques</subject><subject>Infectious diseases</subject><subject>Lymphocyte Activation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Molecular Weight</subject><subject>Onchocerca volvulus - genetics</subject><subject>Onchocerca volvulus - immunology</subject><subject>Onchocerciasis - immunology</subject><subject>Onchocercosis</subject><subject>Parasitic diseases</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - immunology</subject><subject>T-Lymphocytes - immunology</subject><issn>0090-1229</issn><issn>1090-2341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1PwzAMxSMEgvFx5YaUA0Jw6HDipF2OfIM0aZdxnrwshUCbjKadBH89HUxcOdny-_nJfowdCxgKgPzSVj4MhTHFUCmALTYQYCCTqMQ2G8C6F1KaPbaf0hv0CwqKXbZrUGooYMDSOFqq_Be1PgYeSz7lFBb8mltXVTy1vu6qXgsvfBFr8iGtmfbVcV_XXYj90AcKLUfM3m-JL5vYOv9jNAn2NVrXWOKrWK26qkv8fLJCvDhkOyVVyR1t6gF7vr-b3jxm48nD083VOFvKPG8zuXAOCUHIEZF2GrVBZ0YGyNpCIwqhSiW1tWUhNTkBQud2LksAoVCpOR6ws1_f_qqPzqV2Vvu0_ouCi12aFQZhpHP1LyhyqQUK3YMnG7Cb124xWza-puZztomz1083OqU-1rKhYH36w-RIF0ZK_AYY5YKn</recordid><startdate>19971001</startdate><enddate>19971001</enddate><creator>POGONKA, T</creator><creator>BRATTIG, N</creator><creator>NDE, P. 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N</creatorcontrib><creatorcontrib>ADAM, R</creatorcontrib><creatorcontrib>SEEBER, F</creatorcontrib><creatorcontrib>ZIPFEL, P. F</creatorcontrib><creatorcontrib>TITANJI, V. P. K</creatorcontrib><creatorcontrib>LUCIUS, R</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical immunology and immunopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>POGONKA, T</au><au>BRATTIG, N</au><au>NDE, P. N</au><au>ADAM, R</au><au>SEEBER, F</au><au>ZIPFEL, P. F</au><au>TITANJI, V. P. K</au><au>LUCIUS, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localization of T and B cell stimulating domains of the immunodominant 33-kDa protein of Onchocerca volvulus (Ov33)</atitle><jtitle>Clinical immunology and immunopathology</jtitle><addtitle>Clin Immunol Immunopathol</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>85</volume><issue>1</issue><spage>56</spage><epage>66</epage><pages>56-66</pages><issn>0090-1229</issn><eissn>1090-2341</eissn><coden>CLIIAT</coden><abstract>The localization of T and B cell epitopes on a well characterized 33-kDa protein of the filarial nematode Onchocerca volvulus (Ov33) was studied using peripheral blood mononuclear cells (PBMC) and sera from a total of 52 onchocerciasis patients with the generalized form of infection. A proportion of the PBMC samples proliferated in response to recombinant Ov33-GST fusion protein and to fusion free Ov33-6xHis. Proliferative responses of patient PBMC to seven truncated Ov33-6xHis polypeptides and to three synthetic peptides revealed at least one major and two minor T cell epitopes in the protein. The dominant T cell stimulating domain was localized between amino acids 113 and 143. ELISA studies with the Ov33-GST fusion protein revealed that patient sera contained Ov33-specific IgG1, IgG4, IgE, and IgM antibodies. Analysis of the IgG4 response with 10 truncated Ov33 polypeptides identified four B cell stimulating domains in the N-terminal, central, and C-terminal region of the molecule. The B cell domain recognized by the majority of sera was localized between amino acids 113 and 143. The data indicate that this region of the protein is the major T and B cell stimulating domain of Ov33 and might be relevant for vaccine development and for improved immunodiagnosis of onchocerciasis.</abstract><cop>San Diego, CA</cop><cop>New York, NY</cop><cop>Boston</cop><pub>Academic Press</pub><pmid>9325070</pmid><doi>10.1006/clin.1997.4400</doi><tpages>11</tpages></addata></record> |
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subjects | Adolescent Adult Aged Amino Acid Sequence Animals Antibodies, Helminth - blood Antigens, Helminth - chemistry Antigens, Helminth - genetics B-Lymphocytes - immunology Biological and medical sciences Diseases caused by nematodes Female Filariases Helminth Proteins - chemistry Helminth Proteins - genetics Helminth Proteins - immunology Helminthic diseases Humans Immunodominant Epitopes - chemistry Immunodominant Epitopes - genetics In Vitro Techniques Infectious diseases Lymphocyte Activation Male Medical sciences Middle Aged Molecular Sequence Data Molecular Weight Onchocerca volvulus - genetics Onchocerca volvulus - immunology Onchocerciasis - immunology Onchocercosis Parasitic diseases Recombinant Fusion Proteins - chemistry Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - immunology T-Lymphocytes - immunology |
title | Localization of T and B cell stimulating domains of the immunodominant 33-kDa protein of Onchocerca volvulus (Ov33) |
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