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Microbiota-Parasite Interaction: Implication of Secretory Immunoglobulin A and P2X7 Receptor Signaling.
Aboulhoda, Basma Emad; Abdelfatah, Mohamed; El-Wakil, Eman S; Alghamdi, Mansour; Albadawi, Emad A; Hassan, Fatma E; El Saftawy, Enas A.
Afiliação
  • Aboulhoda BE; Department of Anatomy and Embryology, Faculty of Medicine, Cairo University, 11865 Cairo, Egypt.
  • Abdelfatah M; Department of Medical Parasitology, Armed Forces College of Medicine, 11865 Cairo, Egypt.
  • El-Wakil ES; Department of Parasitology, Theodor Bilharz Research Institute, 12411 Giza, Egypt.
  • Alghamdi M; Department of Anatomy, College of Medicine, King Khalid University, 62529 Abha, Saudi Arabia.
  • Albadawi EA; Genomics and Personalized Medicine Unit, College of Medicine, King Khalid University, 62529 Abha, Saudi Arabia.
  • Hassan FE; Department of Anatomy, College of Medicine, Taibah University, 42315 Medinah, Saudi Arabia.
  • El Saftawy EA; Medical Physiology Department, Kasr Alainy, Faculty of Medicine, Cairo University, 11562 Giza, Egypt.
Discov Med ; 36(181): 217-233, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38409828
ABSTRACT
The microbiota community is composed of bacteria, fungi, viruses, and protists that exert symbiotic effects within the human body. Unlike microbiota, parasites are characteristically reliant on their hosts to thrive and flourish, producing toxic metabolites that agitate microbiota and disturb homeostasis. The proper management of parasitic infections addresses several important challenges related to low socioeconomic status and emergent resistance. Therefore, understanding the microbiota's role in interactions with hosts and parasites is crucial for managing parasite diseases with fewer economic and adverse effects associated with pharmaceutical interventions. The current review was divided into three sections. Section 1 focused on the mutual microbiota-host interaction through the purinergic P2X7 receptor (P2X7R) and secretory immunoglobulin A (SIgA). The P2X7R is an abundant intestinal cation channel that is crucial in mucosal immunity, facilitated by SIgA-mediated protection in both innate and adaptive immunity. This study demonstrated that microbiota continually "teach and train" host immunity to attain homeostasis via SIgA production (in T cell-independent and T cell-dependent pathways) and the purinergic receptor P2X7R. In addition, we discussed the potential of manipulating SIgA and P2X7R in immune therapies targeting parasitic infections. Section 2 exhibited parasite-microbiota (microbe-microbe) interactions wherein each can indirectly affect one another through physical and immunogenic alterations and directly via predation, bactericidal protein production, and overlapping of nutrient resources. Thus, microbe-microbe interactions appeared to be multifaceted and species-dependent. Section 3 showed the relationship between microbiota and specific parasites, and the promising role of probiotics. In this section, the review discussed examples of tissue, blood, gastrointestinal, genitourinary, and respiratory parasitic diseases, while highlighting the associated dysbiosis. Furthermore, Section 3 acknowledged the importance of "strain-dependent" biotherapy to boost beneficial microbiota, modulate immunity, and exert anti-parasitic effects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Parasitos / Doenças Parasitárias / Microbiota Limite: Animals / Humans Idioma: En Revista: Discov Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Parasitos / Doenças Parasitárias / Microbiota Limite: Animals / Humans Idioma: En Revista: Discov Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito