Abstract:SUMMARY
Mononuclear cells from peripheral blood (PBMC) of rheumatoid arthritis (RA) patients and healthy controls were incubated with α‐CD3. Cytokine secretion from 2h to 72 h of incubation was measured by ELISA, There were no significant differences in secretion of T cell derived IL‐2 and IL‐4 in cultures from RA patients and controls. The macrophage‐derived cytokines, IL‐1β and tumour‐necrosis factor‐α (TNF‐α) were secreted with a steep increase of concentration during the first 16 h of incubation by PBMC fr… Show more
“…Kinetic experiments were performed to establish the optimum time point for collection and evaluation of the supernatants. The time points obtained (48 hrs for the cytokines IFN-γ, TNF-α, and IL-12, and 24 hours for IL-2) are in agreement with previous reports for healthy controls assayed under similar conditions (48 – 50). All kits were from Biosource International except for IL-2 (R and D Systems).…”
Background-The period just after surgery for breast cancer requires psychosocial adaptation and is associated with elevated distress. Distress states have been associated with decreased cellular immune functioning in this population, which could have negative effects on physical recovery. However little is known about relations between psychological status (negative and positive mood states and overall quality of life) and cellular signaling cytokines that could account for these associations in women undergoing treatment for breast cancer.
“…Kinetic experiments were performed to establish the optimum time point for collection and evaluation of the supernatants. The time points obtained (48 hrs for the cytokines IFN-γ, TNF-α, and IL-12, and 24 hours for IL-2) are in agreement with previous reports for healthy controls assayed under similar conditions (48 – 50). All kits were from Biosource International except for IL-2 (R and D Systems).…”
Background-The period just after surgery for breast cancer requires psychosocial adaptation and is associated with elevated distress. Distress states have been associated with decreased cellular immune functioning in this population, which could have negative effects on physical recovery. However little is known about relations between psychological status (negative and positive mood states and overall quality of life) and cellular signaling cytokines that could account for these associations in women undergoing treatment for breast cancer.
“…IFNγ reaches its maximum at 4–5 days, and IL-1β reaches its maximum level at 24 hr, after which a plateau is attained. (Adapted from (Ruschen et al, 1992; van de Veerdonk et al, 2009))…”
Summary
Gut microbial dysbioses are linked to aberrant immune responses, which are often accompanied by abnormal production of inflammatory cytokines. As part of the Human Functional Genomics Project (HFGP), we investigate how differences in composition and function of gut microbial communities may contribute to inter-individual variation in cytokine responses to microbial stimulations in healthy humans. We observe microbiome-cytokine interaction patterns that are stimulus-specific, cytokine-specific, and cytokine- and stimulus-specific. Validation of two predicted host-microbial interactions reveal that TNFα and IFNγ production are associated with specific microbial metabolic pathways: palmitoleic acid metabolism and tryptophan degradation to tryptophol. Besides providing a resource of predicted microbially-derived mediators that influence immune phenotypes in response to common microorganisms, these data can help to define principles for understanding disease susceptibility. The three HFGP studies presented in this issue lay the groundwork for further studies aimed at understanding the interplay between microbial, genetic, and environmental factors in the regulation of the immune response in humans.
“…In this study, TNFIs were associated with IRIS development, except the immunosuppressive drugs without TNFIs. Interestingly, RA and Crohn's disease are Th1 cell-dominant diseases [20][21][22][23], and TNFI promotes the Th2 cytokine-dominant balance via inhibition of TNF-α. The Th2 cytokine-dominant balance caused by TNFI at the initial treatment of TB may be partly associated with IRIS development.…”
Immune reconstitution inflammatory syndrome (IRIS) is an immune reaction that occurs along with the recovery of the patient’s immunity. Tuberculosis-related IRIS (TB-IRIS) upon tumor necrosis factor (TNF)-α inhibitor treatment has been reported in non-human immunodeficiency virus (HIV) patients. However, the importance of biological treatment, as a risk factor of IRIS, has not yet been established. In this study, we examined TB-IRIS in non-HIV patients to explore the role of TNF-α inhibitor treatment. Out of 188 patients with pulmonary TB, seven patients had IRIS. We examined univariate logistic and multivariate analysis to elucidate risk factors of TB-IRIS. Univariate analysis indicated that usage of immunosuppressive drugs, TNF-α inhibitors, and history of food or drug allergy were significantly related with TB-IRIS. On initial treatment, the values of serological markers such as serum albumin and serum calcium were significantly related with TB-IRIS. There was a higher mortality rate in patients with TB-IRIS. Furthermore, multivariate analysis revealed that usage of TNF-α inhibitors, history of allergy, and serum hypercalcemia were related to TB-IRIS. Usage of TNF-α inhibitors, history of allergy, and serum hypercalcemia may be independent predictors of TB-IRIS in non-HIV patients. Since higher mortality has been reported for TB-IRIS, we should pay attention to TB patients with these risk factors.
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