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What is the Difference Between CTLA-4 and PD-1

9月7, 2023Posted byDr.Samanthi

Thekey differencebetween CTLA-4 and PD-1is that CTLA-4 is a negative regulator ofT-cellimmune function that is thought to suppress T-cell function early in an immune response, while PD-1 is a negative regulator of T-cell immune function that is thought to suppress T-cell function late in animmune response.

Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and programmed death 1 (PD-1) are two different negative regulators of T-cell immune function. Other than inhibiting immune responses, CTLA-4 and PD-1 also have antitumor responses. CTLA-4 is primarily functioning inlymph nodes, while PD-1 is primarily functioning in peripheral tissues. Ipilimumab, nivolumab, and pembrolizumab are drugs that can inhibit the functions of CTLA-4 and PD-1. These are mainly used in cancer treatments such asmelanomaand non-small cell lung cancer.

CONTENTS

1.Overview and Key Difference
2.What is CTLA-4
3.What is PD-1
4.Similarities – CTLA-4 and PD-1
5.CTLA-4 vs. PD-1 in Tabular Form
6.Summary – CTLA-4 vs. PD-1

What is CTLA-4?

CTLA-4 is a molecule that decreases the function of T cells. CTLA-4 is also known as CD152 (cluster of differentiation 152). It is a protein receptor that normally functions as an immune checkpoint. CTLA-4 downregulates immune responses as well. CTLA-4 is a protein encoded by the CTLA-4 gene and contains an extracellular V domain, a transmembrane domain, and a cytoplasmic tail.

CTLA-4 and PD-1 - Side by Side Comparison

Figure 01: CTLA-4

CTLA-4于1991年首次发现。CTLA-4是力宏ologous to the T-cell co-stimulatory protein called CD28. CD28 transmits a stimulatory signal to T cell and enhance T cell immune function. Both CTLA-4 and CD28 bind to CD80 and CD86 (B7-1 and B7-2, respectively) on antigen-presenting cells. But CTLA-4 binds to CD80 and CD86 with greater affinity than CD28. This enables CTLA-4 to outcompete CD28 for its ligands. Thereby, CTLA-4 transmits an inhibitory signal to T cells and downregulates T cell function ultimately. Furthermore, variations in the CTLA-4 gene have been associated with Type 1 diabetes, Graves’ disease, Hashimoto’s thyroiditis, celiac disease, systemic lupus erythematosus, thyroid-associated orbitopathy, primary biliary cirrhosis, and other autoimmune diseases such as rheumatoid arthritis, autoimmune thyroid disease, and multiple sclerosis.

What is PD-1?

Programmed cell death protein 1(PD-1) is an inhibitory receptor protein T cells express during activation. It is also a protein found on the surface ofB cells. PD-1 is a protein in humans which is encoded by thePDCD1gene. Moreover, it is a cell surface receptor that belongs to the immunoglobulin superfamily. PD-1 is a negative regulator of T-cell immune function that is thought to suppress T-cell function late in an immune response. PD-1 primarily functions in peripheral tissues. This protein down-regulates the immune system, and this prevents autoimmune diseases. However, it can also prevent the immune system from killing cancer cells.

CTLA-4 vs PD-1 in Tabular Form

图02:消极,低,高PD-1

PD-1 is an immune checkpoint and guards protein against autoimmunity through two mechanisms. In the first mechanism, PD-1 promotes apoptosis or programmed cell death of antigen-specific T-cells in lymph nodes, whereas, in the second mechanism, PD-1 reduces apoptosis in regulatory T cells (anti-inflammatory or suppressive T cells that maintain tolerance to self-antigens and prevent autoimmune disease). Furthermore, blocking PD-1 is currently used to treat diseases such as cancer, HIV, and Alzheimer’s disease.

What are the Similarities Between CTLA-4 and PD-1?

  • CTLA-4 and PD-1 are two different negative regulators of T-cell immune function.
  • Both are immune checkpoints and guard proteins.
  • Both are cell surface receptors of the immunoglobulin superfamily
  • They are extremely important to control autoimmunity.
  • Ipilimumab, nivolumab, and pembrolizumab are drugs that can inhibit the functions of CTLA-4 and PD-1.

What is the Difference Between CTLA-4 and PD-1?

CTLA-4 is a negative regulator of T-cell immune function that is thought to suppress T-cell function early in an immune response, while PD-1 is a negative regulator of T-cell immune function that is thought to suppress T-cell function late in an immune response. Thus, this is the key difference between CTLA-4 and PD-1. Furthermore, CTLA-4 was first identified in 1991, while PD-1 was first identified in 1992.

The infographic below presents the differences between CTLA-4 and PD-1 in tabular form for side-by-side comparison.

Summary – CTLA-4 vs. PD-1

Immune checkpoints are regulatory molecules of the immune system. These molecules are extremely important for self-tolerance, and they prevent the immune system from attacking one’s own cells indiscriminately. CTLA-4 and PD-1 are two immune checkpoints and guard proteins and are negative regulators of T-cell immune function. CTLA-4 is an immune checkpoint and guard protein that suppresses T-cell function early in an immune response, while PD-1 is an immune checkpoint and guard protein that suppresses T-cell function late in an immune response. So, this summarizes the difference between CTLA-4 and PD-1.

Reference:

1. “CTLA-4.” ScienceDirect Topics.
2.“PMC.” National Center for Biotechnology Information.

Image Courtesy:

1. “11 Hegasy CTLA4 PD1 Immunotherapy” By Guido4 – Own work(CC BY-SA 3.0)via Commons Wikimedia
2. “Negative, low and high PD-L1 expression by immunohistochemistry” By Müller T, Braun M, Dietrich D, Aktekin S, Höft S, Kristiansen G – Müller T, Braun M, Dietrich D, Aktekin S, Höft S, Kristiansen G (2017). “PD-L1: a novel prognostic biomarker in head and neck squamous cell carcinoma”. Oncotarget 8 (32): 52889-52900. DOI:10.18632/oncotarget.17547. PMID 28881780. PMC: 5581079.-(CC BY 3.0)via Commons Wikimedia

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Filed Under:Biology

About the Author:Dr.Samanthi

Dr.Samanthi Udayangani holds a B.Sc. Degree in Plant Science, M.Sc. in Molecular and Applied Microbiology, and PhD in Applied Microbiology. Her research interests include Bio-fertilizers, Plant-Microbe Interactions, Molecular Microbiology, Soil Fungi, and Fungal Ecology.

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