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1.
Clin Immunol ; 187: 26-32, 2018 02.
Artículo en Inglés | MEDLINE | ID: mdl-28863969

RESUMEN

Interleukin-7 is a cytokine essential for T cell homeostasis. IL-7 binds to cellular IL-7 receptors in competition with a soluble form of the receptor (sIL-7Rα). We hypothesized that altered sIL-7Rα levels may cause adverse outcomes in patients undergoing HSCT. In parallel, we investigated the impact of the IL-7Rα SNP rs6897932, which has been associated with release of IL-7R. The sIL-7Rα levels decreased during HSCT (from 114ng/ml before to 48ng/ml at day +14 (P<0.0001)). This pattern was inversely mirrored by IL-7. The IL-7/sIL-7Rα ratio at day +14 was significantly higher in patients developing grades II-IV aGVHD (OR=4.3, P=0.026). Furthermore, donor carriage of the rs6897932 T allele was associated with reduced sIL-7Rα levels, increased risk of grades II-IV aGVHD (OR=2.4, P=0.055) and increased transplant-related mortality (CC=4.5%, CT=21.4% and TT=27.3%, P=0.0037). In conclusion, this study suggests an impact of sIL-7Rα levels and rs6897932 donor genotype on alloreactivity and outcome after HSCT.


Asunto(s)
Enfermedad Injerto contra Huésped/inmunología , Trasplante de Células Madre Hematopoyéticas , Subunidad alfa del Receptor de Interleucina-7/inmunología , Interleucina-7/inmunología , Leucemia/terapia , Linfoma no Hodgkin/terapia , Enfermedades Mielodisplásicas-Mieloproliferativas/terapia , Enfermedad Aguda , Adolescente , Adulto , Anciano , Niño , Preescolar , Femenino , Enfermedad Injerto contra Huésped/epidemiología , Humanos , Lactante , Masculino , Persona de Mediana Edad , Mortalidad , Polimorfismo de Nucleótido Simple , Linfocitos T/inmunología , Trombocitemia Esencial/terapia , Trasplante Homólogo , Adulto Joven
2.
J Immunotoxicol ; 13(2): 270-3, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26181512

RESUMEN

Recent studies suggest that exposure to perfluorinated alkylate substances (PFASs) may induce immunosuppression in humans and animal models. In this exploratory study, 12 healthy adult volunteers were recruited. With each subject, serum-PFAS concentrations were measured and their antibody responses prospectively followed for 30 days after a booster vaccination with diphtheria and tetanus. The results indicated that serum-PFAS concentrations were positively correlated and positively associated with age and male sex. The specific antibody concentrations in serum were increased from Day 4 to Day 10 post-booster, after which a constant concentration was reached. Serum PFAS concentrations showed significant negative associations with the rate of increase in the antibody responses. Interestingly, this effect was particularly strong for the longer-chain PFASs. All significant associations remained significant after adjustment for sex and age. Although the study involved a small number of subjects, these findings of a PFAS-associated reduction of the early humoral immune response to booster vaccination in healthy adults supported previous findings of PFAS immunosuppression in larger cohorts. Furthermore, the results suggested that cellular mechanisms right after antigen exposure should be investigated more closely to identify possible mechanisms of immunosuppression from PFAS.


Asunto(s)
Anticuerpos Antibacterianos/sangre , Formación de Anticuerpos/efectos de los fármacos , Vacuna contra Difteria y Tétanos/administración & dosificación , Exposición a Riesgos Ambientales , Hidrocarburos Fluorados/sangre , Adulto , Femenino , Humanos , Inmunización Secundaria , Masculino
3.
Transplantation ; 91(7): 731-6, 2011 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-21326139

RESUMEN

BACKGROUND: Interleukin-7 (IL-7) is a hematopoietic cytokine essential for T-cell development in the thymus and for the maintenance of peripheral T cells. A previous study of single nucleotide polymorphisms in the exons of IL-7 receptor α-chain (IL-7Rα) in a Danish cohort of patients undergoing allogeneic stem-cell transplantation (SCT) identified donor genotype GG at rs1494555 as a risk factor for treatment-related mortality (TRM) after SCT. METHODS: In this validation study, 116 British and French SCT patients and their donors were investigated by sequence-specific primer polymerase chain reaction. RESULTS: Both donor rs1494555GG genotype and the tightly coupled rs1494558TT genotype were significantly associated with grade 3 to 4 acute graft versus host disease. Although both genotypes tended to be associated with increased TRM, this did not translate into altered overall survival. CONCLUSION: The present data indicate that the IL-7 pathway is associated with alloreactivity in SCT, which is in line with the previously observed association between IL-7Rα single nucleotide polymorphisms and TRM.


Asunto(s)
Trasplante de Células Madre Hematopoyéticas , Polimorfismo de Nucleótido Simple , Receptores de Interleucina-7/genética , Adolescente , Adulto , Niño , Preescolar , Femenino , Genotipo , Enfermedad Injerto contra Huésped/etiología , Trasplante de Células Madre Hematopoyéticas/mortalidad , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Trasplante Homólogo
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