Inflammation
Inflammation and immune response are two critical physiological processes that are intricately related to each other. They are crucial players of the body’s defense system and act to protect against diverse pathogenic and environmental challenges. Inflammation refers to the localized response of the body’s innate immune system to any injury, irritant, or pathogen that causes tissue damage, while the immune system encompasses both innate and adaptive immune responses that target specific antigens to eliminate them from the body.
In recent years, monoclonal antibodies (mAbs) have emerged as a promising therapy for inflammatory-driven diseases. mAbs are engineered antibodies that target specific cytokines, receptors, or immune cells to modulate their activity and reduce inflammation. For example, anti-TNF-α mAbs, such as infliximab and adalimumab, have been approved for the treatment of rheumatoid arthritis, Crohn’s disease, and psoriasis, and have demonstrated significant therapeutic benefits. Another example is anti-IL-17 mAbs, such as secukinumab and ixekizumab, which have been approved for the treatment of psoriatic arthritis and ankylosing spondylitis. The efficacy and safety of these mAb therapies have been extensively researched, with promising results.
Future therapeutic trends for inflammation are focused on developing targeted therapy, such as gene therapy, cell therapy, and small molecule inhibitors. Gene therapy involves introducing genes into the body to modulate cellular activity, while cell therapy involves using modified cells to replace or repair damaged tissues. Small molecule inhibitors target specific inflammatory pathways, such as Janus kinase inhibitors, which block the activity of pro-inflammatory cytokines. Another promising trend is personalized medicine, where the treatment is tailored to the individual’s genetic and epigenetic makeup to optimize efficacy and minimize side effects.
Whilst inflammation plays an essential role in host defense, a chronic, low-grade inflammatory state is a pathological feature of a wide range of chronic conditions, such as type 2 diabetes. This makes inflammation pathway studies an important area of research where the treatment of such diseases is concerned. ELISA remains one of the most popular tools for the accurate quantification of human cytokines involved in the inflammation process. They are ideal companions for:
- Detection of quantitative protein levels in biological fluids
- Validation of biomarker discovery studies
- Assessing immune response for therapeutics
Created with biorender.com.
Krishgen’s range of inflammation related cytokine ELISA markers has over 600+ publications overall.
Pro-Inflammatory Cytokines:
Anti-Inflammatory Cytokines:
Target | Human | Mouse | Rat | Porcine | Rabbit | Bovine | Others |
---|---|---|---|---|---|---|---|
IL-4 | KB1066 | KLM0051 | KLR0133 | KLP0120 | KLX0002 | KLB0036 | KLN0003 (Ca) |
KLY0030 (GP) | |||||||
KLW0032 (Si) | |||||||
KLV0052 (H) | |||||||
KLS0079 (Sh) | |||||||
KLN0003 (Ca) | |||||||
KLH0025 (Ha) | |||||||
KLG0046 (G) | |||||||
KLF0058 (F) | |||||||
KLC0123 (Ch) | |||||||
IL-5 | KB1067 | KLM0050 | KLR0134 | KLP0121 | KLX0181 | KLB2224 | KLY0129 (GP) |
KLW0033 (Si) | |||||||
KLS0052 (Sh) | |||||||
KLN0354 (Ca) | |||||||
KLG0082 (G) | |||||||
KLC0129 (Ch) | |||||||
IL-10 | KB1072 | KBH11265 | KLR0108 | KLP0110 | KLX0004 | KBH12276 | KLN0006 (Ca) |
KLY0032 (GP) | |||||||
KLW0035 (Si) | |||||||
KLT0030 (Fe) | |||||||
KLS0053 (Sh) | |||||||
KLN0006 (Ca) | |||||||
KLH0027 (Ha) | |||||||
KLG0090 (G) | |||||||
KLF0096 (F) | |||||||
IL-13 | KB1076 | KLM0019 | KLR0112 | KLP0112 | KLX0182 | KLB0427 | KLY0128 (GP) |
KLS0080 (Sh) | |||||||
KLH0026 (Ha) | |||||||
KLG0047 (G) | |||||||
TGF beta | KBH11185 | KLM0285 | KLR0778 | KLP0376 | KLX0133 | KLB2049 | KLS0070 (Sh) |
KLH0024 (Ha) | |||||||
KLW0006 (Si) | |||||||
KLN0174 (Ca) |
Chronic Inflammation: A Double-Edged Sword Chronic inflammation, on the other hand, is a persistent and prolonged inflammatory response that can last for months or even years. It is characterized by the infiltration of immune cells, especially macrophages and lymphocytes, into the injured or infected tissue, where they release large amounts of pro-inflammatory cytokines, such as TNF-α, IL-1β, and IL-6. Chronic inflammation can be triggered by prolonged exposure to pathogens, environmental toxins, or autoimmune diseases. It can also be a result of failed attempts to resolve acute inflammation. Although chronic inflammation is essential for tissue repair and remodeling, an excessive and uncontrolled response can lead to tissue damage, fibrosis, and even cancer.
Cytokine Imbalance: A Culprit of Inflammatory-Driven Diseases Cytokines are a family of small, signaling proteins that mediate communication between immune cells and between immune and non-immune cells. They play a crucial role in regulating immune responses, including inflammation. An imbalance in cytokine levels can lead to chronic inflammation and contribute to the pathogenesis of many inflammatory-driven diseases, such as rheumatoid arthritis, lupus, and psoriasis. For example, an overabundance of pro-inflammatory cytokines, such as TNF-α and IL-6, can cause tissue damage and chronic inflammation, while a deficiency in anti-inflammatory cytokines, such as IL-10, can impair the resolution of inflammation and promote chronicity.