Molecular characterisation of Lac s 1, the major allergen from lettuce ( Lactuca sativa)
IgE sensitisation to non-specific lipid transfer proteins (nsLTP), e.g., Pru p 3 the major allergen from peach and most important allergenic LTP, is strongly associated with severe symptoms in food allergic patients. Lac s 1, a member of the nsLTP protein family, was recently identified as major all...
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creator | Hartz, Christina del Mar San Miguel-Moncín, María Cisteró-Bahíma, Anna Fötisch, Kay Metzner, Karin J. Fortunato, Donatella Lidholm, Jonas Vieths, Stefan Scheurer, Stephan |
description | IgE sensitisation to non-specific lipid transfer proteins (nsLTP), e.g., Pru p 3 the major allergen from peach and most important allergenic LTP, is strongly associated with severe symptoms in food allergic patients. Lac s 1, a member of the nsLTP protein family, was recently identified as major allergen in lettuce (
Lactuca sativa), but has not yet been investigated on the molecular basis.
Molecular characterisation and immunological comparison of Lac s 1 to peach allergen Pru p 3.
Lac s 1 cDNA was cloned by RT-PCR and natural (n) Lac s 1 was purified by a two-step chromatography. Protein structure was verified by N-terminal sequencing, mass spectrometry, and circular dichroism spectroscopy. Immunoblotting, ImmunoCAP™, and competitive IgE binding experiments were performed to study the IgE sensitisation pattern and cross-reactivity with Pru p 3. Allergenic potency was analysed by histamine release assay.
Twenty-nine lettuce allergic patients, with or without concomitant peach allergy, and 19 peach allergic patients without lettuce allergy were included in this study. IgE reactivity to lettuce was due to mono-sensitisation to Lac s 1 or cross-reactive glycan structures. Two Lac s 1 isoforms were identified which showed amino acid identitiy (aa-id) of 62% to each other, up to 66% to Pru p 3, and 72% to the N-terminal peptide of plane pollen LTP Pla a 3. The prevalence of IgE binding to nLac s 1 was 90% using lettuce extract in immunoblotting experiments. Enhanced sensitivity was observed in ImmunoCAP™ using purified nLac s 1 in comparison to extracts (93% versus 76%). Although IgE sensitisation to Lac s 1 and Pru p 3 was strongly associated, the two LTPs showed different IgE binding properties. Sensitisation to LTPs does not necessarily reflect the clinical disease, but Lac s 1 was capable of triggering histamine release as shown by positive skin test results in Lac s 1 mono-sensitised patients and by
in vitro mediator release assays.
Purified nLac s 1 will enhance the sensitivity in component resolved diagnosis of lettuce allergy. Similar to other cross-reactive food allergies, exclusive testing of IgE reactivities to LTP cannot be used as biomarker for clinical relevance. Our data provide indirect evidence that Pru p 3 might act as the primary sensitising agent in patients allergic to both lettuce and peach. |
doi_str_mv | 10.1016/j.molimm.2007.01.030 |
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Lactuca sativa), but has not yet been investigated on the molecular basis.
Molecular characterisation and immunological comparison of Lac s 1 to peach allergen Pru p 3.
Lac s 1 cDNA was cloned by RT-PCR and natural (n) Lac s 1 was purified by a two-step chromatography. Protein structure was verified by N-terminal sequencing, mass spectrometry, and circular dichroism spectroscopy. Immunoblotting, ImmunoCAP™, and competitive IgE binding experiments were performed to study the IgE sensitisation pattern and cross-reactivity with Pru p 3. Allergenic potency was analysed by histamine release assay.
Twenty-nine lettuce allergic patients, with or without concomitant peach allergy, and 19 peach allergic patients without lettuce allergy were included in this study. IgE reactivity to lettuce was due to mono-sensitisation to Lac s 1 or cross-reactive glycan structures. Two Lac s 1 isoforms were identified which showed amino acid identitiy (aa-id) of 62% to each other, up to 66% to Pru p 3, and 72% to the N-terminal peptide of plane pollen LTP Pla a 3. The prevalence of IgE binding to nLac s 1 was 90% using lettuce extract in immunoblotting experiments. Enhanced sensitivity was observed in ImmunoCAP™ using purified nLac s 1 in comparison to extracts (93% versus 76%). Although IgE sensitisation to Lac s 1 and Pru p 3 was strongly associated, the two LTPs showed different IgE binding properties. Sensitisation to LTPs does not necessarily reflect the clinical disease, but Lac s 1 was capable of triggering histamine release as shown by positive skin test results in Lac s 1 mono-sensitised patients and by
in vitro mediator release assays.
Purified nLac s 1 will enhance the sensitivity in component resolved diagnosis of lettuce allergy. Similar to other cross-reactive food allergies, exclusive testing of IgE reactivities to LTP cannot be used as biomarker for clinical relevance. Our data provide indirect evidence that Pru p 3 might act as the primary sensitising agent in patients allergic to both lettuce and peach.</description><identifier>ISSN: 0161-5890</identifier><identifier>EISSN: 1872-9142</identifier><identifier>DOI: 10.1016/j.molimm.2007.01.030</identifier><identifier>PMID: 17349693</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Allergens - chemistry ; Allergens - genetics ; Allergens - immunology ; Antigens, Plant - chemistry ; Antigens, Plant - genetics ; Antigens, Plant - immunology ; Base Sequence ; Cloning, Molecular ; Cross Reactions ; DNA, Complementary - analysis ; DNA, Complementary - genetics ; Food Hypersensitivity ; Histamine Release - immunology ; Humans ; IgE ; Immunoglobulin E - immunology ; Lac s 1 ; Lactuca - immunology ; Lactuca sativa ; Lettuce allergy ; LTP ; Molecular Sequence Data ; Non-specific lipid transfer proteins ; Peach allergy ; Plant Proteins - chemistry ; Plant Proteins - genetics ; Plant Proteins - immunology ; Pru p 3 ; Prunus ; Prunus - immunology ; Skin Tests</subject><ispartof>Molecular immunology, 2007-04, Vol.44 (11), p.2820-2830</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-de871ad2a1caf04251c65c4283d75e3bf6f80ededfc9a7ef8d0cc8a4c9cc23853</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0161589007000430$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17349693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hartz, Christina</creatorcontrib><creatorcontrib>del Mar San Miguel-Moncín, María</creatorcontrib><creatorcontrib>Cisteró-Bahíma, Anna</creatorcontrib><creatorcontrib>Fötisch, Kay</creatorcontrib><creatorcontrib>Metzner, Karin J.</creatorcontrib><creatorcontrib>Fortunato, Donatella</creatorcontrib><creatorcontrib>Lidholm, Jonas</creatorcontrib><creatorcontrib>Vieths, Stefan</creatorcontrib><creatorcontrib>Scheurer, Stephan</creatorcontrib><title>Molecular characterisation of Lac s 1, the major allergen from lettuce ( Lactuca sativa)</title><title>Molecular immunology</title><addtitle>Mol Immunol</addtitle><description>IgE sensitisation to non-specific lipid transfer proteins (nsLTP), e.g., Pru p 3 the major allergen from peach and most important allergenic LTP, is strongly associated with severe symptoms in food allergic patients. Lac s 1, a member of the nsLTP protein family, was recently identified as major allergen in lettuce (
Lactuca sativa), but has not yet been investigated on the molecular basis.
Molecular characterisation and immunological comparison of Lac s 1 to peach allergen Pru p 3.
Lac s 1 cDNA was cloned by RT-PCR and natural (n) Lac s 1 was purified by a two-step chromatography. Protein structure was verified by N-terminal sequencing, mass spectrometry, and circular dichroism spectroscopy. Immunoblotting, ImmunoCAP™, and competitive IgE binding experiments were performed to study the IgE sensitisation pattern and cross-reactivity with Pru p 3. Allergenic potency was analysed by histamine release assay.
Twenty-nine lettuce allergic patients, with or without concomitant peach allergy, and 19 peach allergic patients without lettuce allergy were included in this study. IgE reactivity to lettuce was due to mono-sensitisation to Lac s 1 or cross-reactive glycan structures. Two Lac s 1 isoforms were identified which showed amino acid identitiy (aa-id) of 62% to each other, up to 66% to Pru p 3, and 72% to the N-terminal peptide of plane pollen LTP Pla a 3. The prevalence of IgE binding to nLac s 1 was 90% using lettuce extract in immunoblotting experiments. Enhanced sensitivity was observed in ImmunoCAP™ using purified nLac s 1 in comparison to extracts (93% versus 76%). Although IgE sensitisation to Lac s 1 and Pru p 3 was strongly associated, the two LTPs showed different IgE binding properties. Sensitisation to LTPs does not necessarily reflect the clinical disease, but Lac s 1 was capable of triggering histamine release as shown by positive skin test results in Lac s 1 mono-sensitised patients and by
in vitro mediator release assays.
Purified nLac s 1 will enhance the sensitivity in component resolved diagnosis of lettuce allergy. Similar to other cross-reactive food allergies, exclusive testing of IgE reactivities to LTP cannot be used as biomarker for clinical relevance. Our data provide indirect evidence that Pru p 3 might act as the primary sensitising agent in patients allergic to both lettuce and peach.</description><subject>Allergens - chemistry</subject><subject>Allergens - genetics</subject><subject>Allergens - immunology</subject><subject>Antigens, Plant - chemistry</subject><subject>Antigens, Plant - genetics</subject><subject>Antigens, Plant - immunology</subject><subject>Base Sequence</subject><subject>Cloning, Molecular</subject><subject>Cross Reactions</subject><subject>DNA, Complementary - analysis</subject><subject>DNA, Complementary - genetics</subject><subject>Food Hypersensitivity</subject><subject>Histamine Release - immunology</subject><subject>Humans</subject><subject>IgE</subject><subject>Immunoglobulin E - immunology</subject><subject>Lac s 1</subject><subject>Lactuca - immunology</subject><subject>Lactuca sativa</subject><subject>Lettuce allergy</subject><subject>LTP</subject><subject>Molecular Sequence Data</subject><subject>Non-specific lipid transfer proteins</subject><subject>Peach allergy</subject><subject>Plant Proteins - chemistry</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - immunology</subject><subject>Pru p 3</subject><subject>Prunus</subject><subject>Prunus - immunology</subject><subject>Skin Tests</subject><issn>0161-5890</issn><issn>1872-9142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpaTZJ_0EpOvUDandky5Z8CZSQtoENvaTQm1BGo8aLvEolO9B_X5ld6C09zcA87wzMw9hrAbUA0X_a1VMM4zTVDYCqQdTQwjO2EVo11SBk85xtCiaqTg9wwk5z3gFAD333kp0I1cqhH9oN-3kTA-ESbOJ4b5PFmdKY7TzGPY-eby3yzMVHPt8Tn-wuJm5DoPSL9tynOPFA87wg8fcrWjrL1_Cj_XDOXngbMr061jP248vV7eW3avv96_Xl522FsmnnypFWwrrGCrQeZNMJ7Lsy0q1THbV3vvcayJHzOFhFXjtA1FbigNi0umvP2LvD3ocUfy-UZzONGSkEu6e4ZKN1C1KBXMm3T5IKGi0GLf4LikHqclkVUB5ATDHnRN48pHGy6Y8RYFZJZmcOkswqyYAwRVKJvTnuX-4mcv9CRysFuDgAVB73OFIyGUfaI7kxEc7GxfHpC38BI8qkrg</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Hartz, Christina</creator><creator>del Mar San Miguel-Moncín, María</creator><creator>Cisteró-Bahíma, Anna</creator><creator>Fötisch, Kay</creator><creator>Metzner, Karin J.</creator><creator>Fortunato, Donatella</creator><creator>Lidholm, Jonas</creator><creator>Vieths, Stefan</creator><creator>Scheurer, Stephan</creator><general>Elsevier Ltd</general><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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20070401</creationdate><title>Molecular characterisation of Lac s 1, the major allergen from lettuce ( Lactuca sativa)</title><author>Hartz, Christina ; del Mar San Miguel-Moncín, María ; Cisteró-Bahíma, Anna ; Fötisch, Kay ; Metzner, Karin J. ; Fortunato, Donatella ; Lidholm, Jonas ; Vieths, Stefan ; Scheurer, Stephan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-de871ad2a1caf04251c65c4283d75e3bf6f80ededfc9a7ef8d0cc8a4c9cc23853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Allergens - chemistry</topic><topic>Allergens - genetics</topic><topic>Allergens - immunology</topic><topic>Antigens, Plant - chemistry</topic><topic>Antigens, Plant - genetics</topic><topic>Antigens, Plant - immunology</topic><topic>Base Sequence</topic><topic>Cloning, Molecular</topic><topic>Cross Reactions</topic><topic>DNA, Complementary - analysis</topic><topic>DNA, Complementary - genetics</topic><topic>Food Hypersensitivity</topic><topic>Histamine Release - immunology</topic><topic>Humans</topic><topic>IgE</topic><topic>Immunoglobulin E - immunology</topic><topic>Lac s 1</topic><topic>Lactuca - immunology</topic><topic>Lactuca sativa</topic><topic>Lettuce allergy</topic><topic>LTP</topic><topic>Molecular Sequence Data</topic><topic>Non-specific lipid transfer proteins</topic><topic>Peach allergy</topic><topic>Plant Proteins - chemistry</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - immunology</topic><topic>Pru p 3</topic><topic>Prunus</topic><topic>Prunus - immunology</topic><topic>Skin Tests</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hartz, Christina</creatorcontrib><creatorcontrib>del Mar San Miguel-Moncín, María</creatorcontrib><creatorcontrib>Cisteró-Bahíma, Anna</creatorcontrib><creatorcontrib>Fötisch, Kay</creatorcontrib><creatorcontrib>Metzner, Karin J.</creatorcontrib><creatorcontrib>Fortunato, Donatella</creatorcontrib><creatorcontrib>Lidholm, Jonas</creatorcontrib><creatorcontrib>Vieths, Stefan</creatorcontrib><creatorcontrib>Scheurer, Stephan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hartz, Christina</au><au>del Mar San Miguel-Moncín, María</au><au>Cisteró-Bahíma, Anna</au><au>Fötisch, Kay</au><au>Metzner, Karin J.</au><au>Fortunato, Donatella</au><au>Lidholm, Jonas</au><au>Vieths, Stefan</au><au>Scheurer, Stephan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular characterisation of Lac s 1, the major allergen from lettuce ( Lactuca sativa)</atitle><jtitle>Molecular immunology</jtitle><addtitle>Mol Immunol</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>44</volume><issue>11</issue><spage>2820</spage><epage>2830</epage><pages>2820-2830</pages><issn>0161-5890</issn><eissn>1872-9142</eissn><abstract>IgE sensitisation to non-specific lipid transfer proteins (nsLTP), e.g., Pru p 3 the major allergen from peach and most important allergenic LTP, is strongly associated with severe symptoms in food allergic patients. Lac s 1, a member of the nsLTP protein family, was recently identified as major allergen in lettuce (
Lactuca sativa), but has not yet been investigated on the molecular basis.
Molecular characterisation and immunological comparison of Lac s 1 to peach allergen Pru p 3.
Lac s 1 cDNA was cloned by RT-PCR and natural (n) Lac s 1 was purified by a two-step chromatography. Protein structure was verified by N-terminal sequencing, mass spectrometry, and circular dichroism spectroscopy. Immunoblotting, ImmunoCAP™, and competitive IgE binding experiments were performed to study the IgE sensitisation pattern and cross-reactivity with Pru p 3. Allergenic potency was analysed by histamine release assay.
Twenty-nine lettuce allergic patients, with or without concomitant peach allergy, and 19 peach allergic patients without lettuce allergy were included in this study. IgE reactivity to lettuce was due to mono-sensitisation to Lac s 1 or cross-reactive glycan structures. Two Lac s 1 isoforms were identified which showed amino acid identitiy (aa-id) of 62% to each other, up to 66% to Pru p 3, and 72% to the N-terminal peptide of plane pollen LTP Pla a 3. The prevalence of IgE binding to nLac s 1 was 90% using lettuce extract in immunoblotting experiments. Enhanced sensitivity was observed in ImmunoCAP™ using purified nLac s 1 in comparison to extracts (93% versus 76%). Although IgE sensitisation to Lac s 1 and Pru p 3 was strongly associated, the two LTPs showed different IgE binding properties. Sensitisation to LTPs does not necessarily reflect the clinical disease, but Lac s 1 was capable of triggering histamine release as shown by positive skin test results in Lac s 1 mono-sensitised patients and by
in vitro mediator release assays.
Purified nLac s 1 will enhance the sensitivity in component resolved diagnosis of lettuce allergy. Similar to other cross-reactive food allergies, exclusive testing of IgE reactivities to LTP cannot be used as biomarker for clinical relevance. Our data provide indirect evidence that Pru p 3 might act as the primary sensitising agent in patients allergic to both lettuce and peach.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17349693</pmid><doi>10.1016/j.molimm.2007.01.030</doi><tpages>11</tpages></addata></record> |
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subjects | Allergens - chemistry Allergens - genetics Allergens - immunology Antigens, Plant - chemistry Antigens, Plant - genetics Antigens, Plant - immunology Base Sequence Cloning, Molecular Cross Reactions DNA, Complementary - analysis DNA, Complementary - genetics Food Hypersensitivity Histamine Release - immunology Humans IgE Immunoglobulin E - immunology Lac s 1 Lactuca - immunology Lactuca sativa Lettuce allergy LTP Molecular Sequence Data Non-specific lipid transfer proteins Peach allergy Plant Proteins - chemistry Plant Proteins - genetics Plant Proteins - immunology Pru p 3 Prunus Prunus - immunology Skin Tests |
title | Molecular characterisation of Lac s 1, the major allergen from lettuce ( Lactuca sativa) |
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