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CartBovine IL-2 Polyclonal Antibody - Biotinylated
Reactivity - ELISA
Bovine IL-2 - Strong
Canine IL-2 - None
Chicken IL-2 - None
Cynomolgus Monkey IL-2 - None
Dolphin IL-2 - None
Equine IL-2 - None
Feline IL-2 - None
Human IL-2 - None
Mouse IL-2 - None
Ovine IL-2 - Weak
Rabbit IL-2 - None
Swine IL-2 - None
Bovine IL-2 ELISA Data
Lactation stage impacts the glycolytic function of bovine CD4+ T cells during ex vivo activation.
Eder JM, Gorden PJ, Lippolis JD, Reinhardt TA, Sacco RE.
Sci Rep. 2020 Mar 4;10(1):4045. doi: 10.1038/s41598-020-60691-2.
Applications: Measurement of bovine TNF alpha, IL-2, and IFN gamma in culture supernatants by ELISA
Abstract
Dairy cattle undergo dynamic physiological changes over the course of a full lactation into the dry period, which impacts their immunocompetence. During activation, T cells undergo a characteristic rewiring to increase the uptake of glucose and metabolically reprogram to favor aerobic glycolysis over oxidative phosphorylation. To date it remains to be completely elucidated how the altered energetic demands associated with lactation in dairy cows impacts T cell metabolic reprogramming. Thus, in our ex vivo studies we have examined the influence of stage of lactation (early lactation into the dry period) on cellular metabolism in activated bovine CD4+ T cells. Results showed higher rates of glycolytic function in activated CD4+ T cells from late lactation and dry cows compared to cells from early and mid-lactation cows. Similarly, protein and mRNA expression of cytokines were higher in CD4+ T cells from dry cows than CD4+ T cells from lactating cows. The data suggest CD4+ T cells from lactating cows have an altered metabolic responsiveness that could impact the immunocompetence of these animals, particularly those in early lactation, and increase their susceptibility to infection.
The chronic stages of bovine Fasciola hepatica are dominated by CD4 T-cell exhaustion
Sachdev D, Gough KC, Flynn RJ.
J Immunol. 2014 Jul 15;193(2):597-609
Applications: Bovine IL-2 was used to stimulate cells. Bovine IL-2 and IL-13 were measure in cell culture supernatants by ELISA.
Abstract
Fasciola hepatica infection of ruminants leads to non-resolving chronic infection, as patency develops, there is switching to a TGF-β and IL-10 led response. Here, we explore the responses of CD4 T-cells within the major draining lymph nodes. We found minimal expression of Foxp3 within CD4 cells but elevated levels within the γδ (WC1+) population. There is a strong T-cell-intrinsic exhaustion phenotype within the hepatic lymph node (HLN) characterized by a lack of antigen-specific proliferation and cytokine secretion. CD4 T-cells recovered from the HLN had high levels of PD-1 expression and low levels of IL-2 secretion. Exogenous IL-2 partially rescued this defect; when combined with neutralization of IL-10 and TGF-β, full restoration of proliferation, and cytokine production was achieved. Moreover, there is a clear uncoupling of the mechanisms that facilitate this regulation with parasite-specific proliferation and cytokine secretion being governed by independent means. These data would suggest that there is a CD4 T-cell-intrinsic regulation in place early in chronic infection, potentially leading to failure in resistance to reinfection.
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