Immunomodulatory interventions in myocardial infarction and heart failure: a systematic review of clinical trials and meta-analysis of IL-1 inhibition

Autor: Angelos Papanikolaou, Susanne Sattler, Mona Panahi, Muneer G. Hasham, Nadia Rosenthal, Ji-Gang Zhang, Azam Torabi, Ali Vazir, John G.F. Cleland, Habib Khan, Sian E. Harding
Přispěvatelé: British Heart Foundation
Rok vydání: 2018
Předmět:
0301 basic medicine
Cardiac & Cardiovascular Systems
MONOCLONAL-ANTIBODY
Physiology
medicine.medical_treatment
Anti-Inflammatory Agents
Myocardial Infarction
030204 cardiovascular system & hematology
Bioinformatics
RANDOMIZED DOUBLE-BLIND
0302 clinical medicine
Risk Factors
Medicine
1102 Cardiorespiratory Medicine and Haematology
TUMOR-NECROSIS-FACTOR
Clinical Trials as Topic
biology
C-REACTIVE PROTEIN
VENTRICULAR-FUNCTION
Cytokine
Treatment Outcome
CORONARY ANGIOPLASTY
Immunotherapy
medicine.symptom
Inflammation Mediators
Cardiology and Cardiovascular Medicine
Life Sciences & Biomedicine
Immunosuppressive Agents
Signal Transduction
ACUTE MYOCARDIAL-INFARCTION
Reviews
Inflammation
Proinflammatory cytokine
Immunomodulation
03 medical and health sciences
Immune system
Physiology (medical)
INTRAVENOUS IMMUNOGLOBULIN
Humans
Heart Failure
Science & Technology
business.industry
C-reactive protein
HOSPITAL CARDIAC-ARREST
N-ACETYLCYSTEINE
Blockade
Clinical trial
IL-1 inhibition
Editor's Choice
030104 developmental biology
Cardiovascular System & Hematology
biology.protein
Cardiovascular System & Cardiology
Systematic review
business
Interleukin-1
Zdroj: Cardiovascular Research
ISSN: 1755-3245
0008-6363
Popis: Following a myocardial infarction (MI), the immune system helps to repair ischaemic damage and restore tissue integrity, but excessive inflammation has been implicated in adverse cardiac remodelling and development towards heart failure (HF). Pre-clinical studies suggest that timely resolution of inflammation may help prevent HF development and progression. Therapeutic attempts to prevent excessive post-MI inflammation in patients have included pharmacological interventions ranging from broad immunosuppression to immunomodulatory approaches targeting specific cell types or factors with the aim to maintain beneficial aspects of the early post-MI immune response. These include the blockade of early initiators of inflammation including reactive oxygen species and complement, inhibition of mast cell degranulation and leucocyte infiltration, blockade of inflammatory cytokines, and inhibition of adaptive B and T-lymphocytes. Herein, we provide a systematic review on post-MI immunomodulation trials and a meta-analysis of studies targeting the inflammatory cytokine Interleukin-1. Despite an enormous effort into a significant number of clinical trials on a variety of targets, a striking heterogeneity in study population, timing and type of treatment, and highly variable endpoints limits the possibility for meaningful meta-analyses. To conclude, we highlight critical considerations for future studies including (i) the therapeutic window of opportunity, (ii) immunological effects of routine post-MI medication, (iii) stratification of the highly diverse post-MI patient population, (iv) the potential benefits of combining immunomodulatory with regenerative therapies, and at last (v) the potential side effects of immunotherapies.
Databáze: OpenAIRE