Humoral and cellular responses to SARS-CoV-2 in patients with B-cell haematological malignancies improve with successive vaccination
Patients with haematological malignancies are more likely to have poor responses to vaccination. Here we provide detailed analysis of the humoral and cellular responses to COVID-19 vaccination in 69 patients with B-cell malignancies. Measurement of anti-spike IgG in serum demonstrated a low seroconv...
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Veröffentlicht in: | British journal of haematology 2023-09, Vol.202 (6), p.1091-1103 |
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creator | Pinder, Christopher L Jankovic, Dylan Fox, Thomas A Kirkwood, Amy Enfield, Louise Alrubayyi, Aljawharah Touizer, Emma Ford, Rosemarie Pocock, Rachael Shin, Jin-Sup Ziegler, Joseph Thomson, Kirsty J Ardeshna, Kirit M Peppa, Dimitra McCoy, Laura E Morris, Emma C |
description | Patients with haematological malignancies are more likely to have poor responses to vaccination. Here we provide detailed analysis of the humoral and cellular responses to COVID-19 vaccination in 69 patients with B-cell malignancies. Measurement of anti-spike IgG in serum demonstrated a low seroconversion rate with 27.1% and 46.8% of patients seroconverting after the first and second doses of vaccine, respectively. In vitro pseudoneutralisation assays demonstrated a poor neutralising response, with 12.5% and 29.5% of patients producing a measurable neutralising titre after the first and second doses, respectively. A third dose increased seropositivity to 54.3% and neutralisation to 51.5%, while a fourth dose further increased both seropositivity and neutralisation to 87.9%. Neutralisation titres post-fourth dose showed a positive correlation with the size of the B-cell population measured by flow cytometry, suggesting an improved response correlating with recovery of the B-cell compartment after B-cell depletion treatments. In contrast, interferon gamma ELISpot analysis showed a largely intact T-cell response, with the percentage of patients producing a measurable response boosted by the second dose to 75.5%. This response was maintained thereafter, with only a small increase following the third and fourth doses, irrespective of the serological response at these timepoints. |
doi_str_mv | 10.1111/bjh.18962 |
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Here we provide detailed analysis of the humoral and cellular responses to COVID-19 vaccination in 69 patients with B-cell malignancies. Measurement of anti-spike IgG in serum demonstrated a low seroconversion rate with 27.1% and 46.8% of patients seroconverting after the first and second doses of vaccine, respectively. In vitro pseudoneutralisation assays demonstrated a poor neutralising response, with 12.5% and 29.5% of patients producing a measurable neutralising titre after the first and second doses, respectively. A third dose increased seropositivity to 54.3% and neutralisation to 51.5%, while a fourth dose further increased both seropositivity and neutralisation to 87.9%. Neutralisation titres post-fourth dose showed a positive correlation with the size of the B-cell population measured by flow cytometry, suggesting an improved response correlating with recovery of the B-cell compartment after B-cell depletion treatments. In contrast, interferon gamma ELISpot analysis showed a largely intact T-cell response, with the percentage of patients producing a measurable response boosted by the second dose to 75.5%. This response was maintained thereafter, with only a small increase following the third and fourth doses, irrespective of the serological response at these timepoints.</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/bjh.18962</identifier><identifier>PMID: 37402627</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Antibodies, Viral ; Cell size ; COVID-19 ; COVID-19 - prevention & control ; COVID-19 Vaccines ; Enzyme-linked immunosorbent assay ; Flow cytometry ; Hematologic Neoplasms - therapy ; Hematology ; Humans ; Immunization ; Immunoglobulin G ; Malignancy ; Original Paper ; SARS-CoV-2 ; Seroconversion ; Severe acute respiratory syndrome coronavirus 2 ; Vaccination</subject><ispartof>British journal of haematology, 2023-09, Vol.202 (6), p.1091-1103</ispartof><rights>2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 The Authors. published by British Society for Haematology and John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-c04a1816dc1b29e488d0217c164c3094d9fca86a82606e6d22baeabba720b9bb3</citedby><cites>FETCH-LOGICAL-c404t-c04a1816dc1b29e488d0217c164c3094d9fca86a82606e6d22baeabba720b9bb3</cites><orcidid>0000-0002-1163-2295 ; 0000-0001-9503-7946 ; 0000-0003-4149-226X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37402627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pinder, Christopher L</creatorcontrib><creatorcontrib>Jankovic, Dylan</creatorcontrib><creatorcontrib>Fox, Thomas A</creatorcontrib><creatorcontrib>Kirkwood, Amy</creatorcontrib><creatorcontrib>Enfield, Louise</creatorcontrib><creatorcontrib>Alrubayyi, Aljawharah</creatorcontrib><creatorcontrib>Touizer, Emma</creatorcontrib><creatorcontrib>Ford, Rosemarie</creatorcontrib><creatorcontrib>Pocock, Rachael</creatorcontrib><creatorcontrib>Shin, Jin-Sup</creatorcontrib><creatorcontrib>Ziegler, Joseph</creatorcontrib><creatorcontrib>Thomson, Kirsty J</creatorcontrib><creatorcontrib>Ardeshna, Kirit M</creatorcontrib><creatorcontrib>Peppa, Dimitra</creatorcontrib><creatorcontrib>McCoy, Laura E</creatorcontrib><creatorcontrib>Morris, Emma C</creatorcontrib><title>Humoral and cellular responses to SARS-CoV-2 in patients with B-cell haematological malignancies improve with successive vaccination</title><title>British journal of haematology</title><addtitle>Br J Haematol</addtitle><description>Patients with haematological malignancies are more likely to have poor responses to vaccination. Here we provide detailed analysis of the humoral and cellular responses to COVID-19 vaccination in 69 patients with B-cell malignancies. Measurement of anti-spike IgG in serum demonstrated a low seroconversion rate with 27.1% and 46.8% of patients seroconverting after the first and second doses of vaccine, respectively. In vitro pseudoneutralisation assays demonstrated a poor neutralising response, with 12.5% and 29.5% of patients producing a measurable neutralising titre after the first and second doses, respectively. A third dose increased seropositivity to 54.3% and neutralisation to 51.5%, while a fourth dose further increased both seropositivity and neutralisation to 87.9%. Neutralisation titres post-fourth dose showed a positive correlation with the size of the B-cell population measured by flow cytometry, suggesting an improved response correlating with recovery of the B-cell compartment after B-cell depletion treatments. In contrast, interferon gamma ELISpot analysis showed a largely intact T-cell response, with the percentage of patients producing a measurable response boosted by the second dose to 75.5%. This response was maintained thereafter, with only a small increase following the third and fourth doses, irrespective of the serological response at these timepoints.</description><subject>Antibodies, Viral</subject><subject>Cell size</subject><subject>COVID-19</subject><subject>COVID-19 - prevention & control</subject><subject>COVID-19 Vaccines</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Flow cytometry</subject><subject>Hematologic Neoplasms - therapy</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunization</subject><subject>Immunoglobulin G</subject><subject>Malignancy</subject><subject>Original Paper</subject><subject>SARS-CoV-2</subject><subject>Seroconversion</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Vaccination</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUFvFCEYhonR2LV68A8YEi96mMoHLMOcTN1o26SJiVWv5BuG3WUzAyPMrPHeHy7rto3KhRAennwvLyEvgZ1BWe_a3fYMdKP4I7IAoZYVBwmPyYIxVlfApD4hz3LeMQaCLeEpORG1ZFzxekFuL-chJuwpho5a1_dzj4kml8cYsst0ivTm_MtNtYrfK059oCNO3oUp059-2tIP1eEN3aIbcIp93HhbXAP2fhMwWF8MfhhT3Lsjn2drXc6-nPdorQ_FFsNz8mSNfXYv7vZT8u3Tx6-ry-r688XV6vy6spLJqbJMImhQnYWWN05q3TEOtQUlrWCN7Jq1Ra1Qc8WUUx3nLTpsW6w5a5u2Fafk_dE7zu3gOltylOhmTH7A9MtE9Obfm-C3ZhP3BlizFGIJxfDmzpDij9nlyQw-H74Ag4tzNlwLoaRS8oC-_g_dxTmFkq9QSoBWTV0X6u2RsinmnNz6YRpg5lCuKeWaP-UW9tXf4z-Q922K36RwogE</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Pinder, Christopher L</creator><creator>Jankovic, Dylan</creator><creator>Fox, Thomas A</creator><creator>Kirkwood, Amy</creator><creator>Enfield, Louise</creator><creator>Alrubayyi, Aljawharah</creator><creator>Touizer, Emma</creator><creator>Ford, Rosemarie</creator><creator>Pocock, Rachael</creator><creator>Shin, Jin-Sup</creator><creator>Ziegler, Joseph</creator><creator>Thomson, Kirsty J</creator><creator>Ardeshna, Kirit M</creator><creator>Peppa, Dimitra</creator><creator>McCoy, Laura E</creator><creator>Morris, Emma C</creator><general>Blackwell Publishing Ltd</general><general>John Wiley and Sons Inc</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1163-2295</orcidid><orcidid>https://orcid.org/0000-0001-9503-7946</orcidid><orcidid>https://orcid.org/0000-0003-4149-226X</orcidid></search><sort><creationdate>20230901</creationdate><title>Humoral and cellular responses to SARS-CoV-2 in patients with B-cell haematological malignancies improve with successive vaccination</title><author>Pinder, Christopher L ; 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Here we provide detailed analysis of the humoral and cellular responses to COVID-19 vaccination in 69 patients with B-cell malignancies. Measurement of anti-spike IgG in serum demonstrated a low seroconversion rate with 27.1% and 46.8% of patients seroconverting after the first and second doses of vaccine, respectively. In vitro pseudoneutralisation assays demonstrated a poor neutralising response, with 12.5% and 29.5% of patients producing a measurable neutralising titre after the first and second doses, respectively. A third dose increased seropositivity to 54.3% and neutralisation to 51.5%, while a fourth dose further increased both seropositivity and neutralisation to 87.9%. Neutralisation titres post-fourth dose showed a positive correlation with the size of the B-cell population measured by flow cytometry, suggesting an improved response correlating with recovery of the B-cell compartment after B-cell depletion treatments. In contrast, interferon gamma ELISpot analysis showed a largely intact T-cell response, with the percentage of patients producing a measurable response boosted by the second dose to 75.5%. This response was maintained thereafter, with only a small increase following the third and fourth doses, irrespective of the serological response at these timepoints.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>37402627</pmid><doi>10.1111/bjh.18962</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-1163-2295</orcidid><orcidid>https://orcid.org/0000-0001-9503-7946</orcidid><orcidid>https://orcid.org/0000-0003-4149-226X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies, Viral Cell size COVID-19 COVID-19 - prevention & control COVID-19 Vaccines Enzyme-linked immunosorbent assay Flow cytometry Hematologic Neoplasms - therapy Hematology Humans Immunization Immunoglobulin G Malignancy Original Paper SARS-CoV-2 Seroconversion Severe acute respiratory syndrome coronavirus 2 Vaccination |
title | Humoral and cellular responses to SARS-CoV-2 in patients with B-cell haematological malignancies improve with successive vaccination |
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