Key result
B-cells and humoral immunity drive cardiac inflammation in heart failure, highlighting potential novel therapeutic targets.
Why the study?
Despite available treatments, CVD and HF remain a leading cause of death worldwide, creating an urgent need to identify novel therapeutic targets. Understanding the specific role of B-cells and humoral immunity in cardiac inflammation may inform new treatment strategies for HF.
This review highlights the pathophysiological role of B-cells and humoral immunity in cardiac inflammation in heart failure, suggesting potential novel therapeutic targets.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for B-cell targeted therapies in heart failure; prospective trials needed before clinical adoption.
Cardiovascular Disease (CVD) is a class of diseases that involve disorders of heart and blood vessels, including hypertension, coronary heart disease, cerebrovascular disease, peripheral vascular disease, which finally lead to Heart Failure (HF). There are several treatments available all over the world, but still, CVD and heart failure became the number one problem causing death every year worldwide. Both experimental and clinical studies have shown a role for inflammation in the pathogenesis of heart failure. This seems related to an imbalance between pro-inflammatory and anti-inflammatory cytokines. Cardiac inflammation is a major pathophysiological mechanism operating in the failing heart, regardless of HF aetiology. Disturbances of the cellular and humoral immune system are frequently observed in heart failure. This review describes how B-cells play a specific role in the heart failure states. There is an urgent need to identify novel therapeutic targets and develop advanced therapeutic strategies to combat the syndrome of HF. Understanding and describing the elements of the humoral immunity function are essential and may suggest potential new treatment strategies.
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Sarkar et al. (2018) conducted a review in Heart failure. Humoral immunity and B-cells was evaluated. B-cells and humoral immunity play a specific pathophysiological role in cardiac inflammation and heart failure states, offering potential novel therapeutic targets.
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