Publication:
Prevalence of Pneumocystosis in Sub-Saharan Africa and Helminth Immune Modulation.

dc.contributor.authorFonte, Luis
dc.contributor.authorGinori, María
dc.contributor.authorCalderon, Enrique J
dc.contributor.authorde Armas, Yaxsier
dc.contributor.funderInstitute of Health Carlos III,
dc.contributor.funderSpanish Ministry of Science, Innovation and University
dc.date.accessioned2023-05-03T14:11:11Z
dc.date.available2023-05-03T14:11:11Z
dc.date.issued2021-12-31
dc.description.abstractSub-Saharan Africa is the region of the world with the highest prevalence of helminth infections. To protect themselves from the defensive mechanisms of their respective hosts, helminths modulate their immune responses. This modulation has relevant clinical and epidemiological consequences, including the inhibition of inflammatory processes that characterize infection by other microorganisms. Severe Pneumocystis pneumonia is characterized by an intense inflammatory reaction that can lead to death. Acquired immunodeficiency syndrome is the main predisposing factor to the development of pneumocystosis. Although the introduction of highly active antiretroviral therapy has led to a notable decline in the incidence of acquired immunodeficiency syndrome-associated complications, pneumocystosis continues to be an important global health problem. Despite the high incidence of human immunodeficiency virus infection in the sub-Saharan region, the prevalence of Pneumocystis pneumonia there has been lower than expected. Several factors, or combinations thereof, may contribute to this evolution. Here, we hypothesize the possible role of helminth immune modulation as an important issue at play. On the other hand, and looking ahead, we believe that the immune modulation achieved by helminths may be an important factor to consider during the design and evaluation processes of vaccines against Pneumocystis jirovecii to be used in Sub-Saharan Africa. The requirements of a balanced triggering of different types of immune responses for controlling the infection produced by this microorganism, as observed during experiments in animal models, support this final consideration.
dc.description.versionSi
dc.identifier.citationFonte L, Ginori M, Calderón EJ, de Armas Y. Prevalence of Pneumocystosis in Sub-Saharan Africa and Helminth Immune Modulation. J Fungi (Basel). 2021 Dec 31;8(1):45.
dc.identifier.doi10.3390/jof8010045
dc.identifier.essn2309-608X
dc.identifier.pmcPMC8779910
dc.identifier.pmid35049985
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779910/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2309-608X/8/1/45/pdf?version=1641269119
dc.identifier.urihttp://hdl.handle.net/10668/21367
dc.issue.number1
dc.journal.titleJournal of fungi (Basel, Switzerland)
dc.journal.titleabbreviationJ Fungi (Basel)
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.page.number5
dc.provenanceRealizada la curación de contenido 20/02/2025
dc.publisherMDPI AG
dc.pubmedtypeJournal Article
dc.relation.projectIDFIS-PI19/01845
dc.relation.publisherversionhttps://www.mdpi.com/resolver?pii=jof8010045
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHIV infection
dc.subjectPneumocystis pneumonia
dc.subjectSub-Saharan Africa
dc.subjecthelminth immune modulation
dc.subjectpneumocystosis
dc.subject.decsHelmintos
dc.subject.decsInfecciones
dc.subject.decsNeumonía por Pneumocystis
dc.subject.decsIncidencia
dc.subject.decsInmunidad
dc.subject.decsPrevalencia
dc.subject.decsVIH
dc.subject.decsPlomo
dc.subject.decsVacunas
dc.subject.meshAcquired Immunodeficiency Syndrome
dc.subject.meshAfrica South of the Sahara
dc.subject.meshHand
dc.subject.meshGlobal Health
dc.subject.meshPneumocystis carinii
dc.subject.meshLead
dc.subject.meshModels, Animal
dc.subject.meshDeath
dc.titlePrevalence of Pneumocystosis in Sub-Saharan Africa and Helminth Immune Modulation.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number8
dspace.entity.typePublication

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