Typhim vi immunization assists to discriminate primary antibody responses in hematological malignancies.

Hematological Malignancies Pneumo 23 Primary responses ROC curve Typhim Vi Union index, cut-off value Youden index secondary responses specific polysaccharide Ab response

Journal

MethodsX
ISSN: 2215-0161
Titre abrégé: MethodsX
Pays: Netherlands
ID NLM: 101639829

Informations de publication

Date de publication:
2020
Historique:
received: 05 12 2019
accepted: 20 05 2020
entrez: 20 6 2020
pubmed: 20 6 2020
medline: 20 6 2020
Statut: epublish

Résumé

Assessment of specific antibody (Ab) production to polysaccharide antigens is clinically relevant, identifying patients at risk for infection by encapsulated bacteria and thus enabling a more rigorous selection of patients that can benefit of immunoglobulin replacement therapy. Classically, the gold-standard test is the measurement of antibody production to pure polysaccharide pneumococcal (PPV) immunization. Several factors, including introduction of conjugate vaccination schedule, serotyping analysis, high baseline Ab levels, have hindered the evaluation of polysaccharide antigens. This is even more difficult in secondary immunodeficiencies (SID), where patients can show secondary responses despite lack of primary antibody responses and present with recurrent or severe infections. Assessment of specific Ab production to pure S

Identifiants

pubmed: 32551240
doi: 10.1016/j.mex.2020.100936
pii: S2215-0161(20)30156-4
pii: 100936
pmc: PMC7289764
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100936

Informations de copyright

© 2020 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

J Ochoa-Grullón (J)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.
Department of Immunology, Ophthalmology and ENT, School of Medicine, Complutense University School of Medicine, Madrid, Spain.
Immunodeficiency Interdepartmental Group (GIID), Madrid, Spain.

C Orte (C)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.

A Rodríguez de la Peña (A)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.

K Guevara-Hoyer (K)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.
Department of Immunology, Ophthalmology and ENT, School of Medicine, Complutense University School of Medicine, Madrid, Spain.
Immunodeficiency Interdepartmental Group (GIID), Madrid, Spain.

G Cordero Torres (G)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.

M Fernández-Arquero (M)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.

I Serrano-García (I)

Department of Epidemiology and Preventive Medicine, Hospital Clínico San Carlos, Madrid, Spain.

M J Recio (MJ)

Immunodeficiency Interdepartmental Group (GIID), Madrid, Spain.
Laboratory of Immunogenetics of Human Diseases, IdiPAZ Institute for Health Research, Madrid, Spain.

R Pérez de Diego (R)

Immunodeficiency Interdepartmental Group (GIID), Madrid, Spain.
Laboratory of Immunogenetics of Human Diseases, IdiPAZ Institute for Health Research, Madrid, Spain.

S Sánchez-Ramón (S)

Department of Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.
Department of Immunology, Ophthalmology and ENT, School of Medicine, Complutense University School of Medicine, Madrid, Spain.
Immunodeficiency Interdepartmental Group (GIID), Madrid, Spain.

Classifications MeSH