Research and Reports in Immunology

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.
Reach Us +1 (202) 780-3397

Perspective - Research and Reports in Immunology (2023) Volume 6, Issue 3

Regulatory T Cells: Maintaining Balance in Adaptive Immune Responses

Michael Gale*

Department of Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom

*Corresponding Author:
Michael Gale
Department of Cardiovascular Science
University of Edinburgh, Edinburgh, United Kingdom
E-mail: Michaelgale@gmail.com

Received: 16-May-2023, Manuscript No. AARRI-23-101833; Editor assigned: 19-May-2023, Pre QC No. AARRI-23-101833(PQ); Reviewed: 02-Jun-2023, QC No. AARRI-23-101833; Revised: 06-Jun-2023, Manuscript No. AARRI-23-101833(R); Published: 13-Jun-2023, DOI:10.35841/aajfnh-6.3.147

Citation: Gale M. Regulatory T cells: maintaining balance in adaptive immune responses. Res Rep Immunol. 2023; 6(3):147

Visit for more related articles at Research and Reports in Immunology

Introduction

Adaptive immunity relies on two main types of cells: B cells and T cells. Both originate from stem cells in the bone marrow and undergo maturation processes to develop their unique functionalities. B cells are responsible for producing antibodies, specialized proteins that recognize and bind to specific antigens present on the surface of pathogens. Each B cell carries a unique receptor that allows it to recognize a particular antigen. When a B cell encounters its matching antigen, it becomes activated, leading to the production and release of large quantities of antibodies. These antibodies neutralize pathogens, mark them for destruction by other immune cells, and prevent their re-entry into the body [1,2].

T cells: T cells are divided into two main types: helper T cells (CD4+) and cytotoxic T cells (CD8+). Helper T cells coordinate immune responses by releasing signaling molecules called cytokines, which activate other immune cells, including B cells and cytotoxic T cells. They also play a crucial role in regulating the immune response. Cytotoxic T cells, on the other hand, directly target and destroy infected cells or cells that display abnormal characteristics, such as cancer cells or cells infected with intracellular pathogens.

Adaptive immunity employs diverse mechanisms to effectively combat pathogens and maintain long-term protection.

Clonal Selection: When a pathogen enters the body, B cells and T cells with matching receptors are activated through a process known as clonal selection. This leads to the proliferation of specific B and T cell clones, amplifying the immune response against the invading pathogen [3].

Antibody Production: B cells produce antibodies, also known as immunoglobulin (Ig), which binds to specific antigens. Antibodies can neutralize pathogens by preventing their entry into host cells or by facilitating their destruction by other immune cells. The production of antibodies by B cells is a critical aspect of the humoral immune response.

Cell-Mediated Immunity: T cells play a vital role in cellmediated immunity. Cytotoxic T cells recognize and destroy infected or abnormal cells directly. They release toxic molecules that induce apoptosis, leading to the elimination of the targeted cells. Helper T cells, meanwhile, stimulate and coordinate the immune response by activating other immune cells and secreting cytokines [4].

Memory Response: One of the most remarkable aspects of adaptive immunity is its ability to develop immunological memory. After an initial encounter with a pathogen, a subset of B and T cells called memory cells is formed. Memory cells "remember" the pathogen, allowing for a rapid and robust immune response upon re-exposure. This is the basis for vaccination, where harmless fragments of pathogens are introduced to stimulate the production of memory cells, providing future protection against the actual pathogen.

Regulatory Mechanisms: To prevent excessive immune responses and autoimmune reactions, the immune system employs regulatory mechanisms. Regulatory T cells (Tregs) are specialized T cells that suppress the immune response, maintaining a balance between protective immunity and tolerance to self-antigens. These cells play a crucial role in preventing autoimmune diseases and maintaining immune homeostasis [5].

Conclusion

Adaptive immunity is a remarkable defense system that provides specific and long-lasting protection against pathogens. The interplay between B cells and T cells, along with the production of antibodies and the development of immunological memory, ensures an effective immune response tailored to each encountered threat. By understanding the intricacies of adaptive immunity, researchers can design more effective vaccines and therapies to combat infectious diseases and improve overall health. Continued research in this field holds the promise of unlocking new ways to harness the power of adaptive immunity and enhance our ability to fight off pathogens.

References

  1. Pelus LM. Peripheral blood stem cell mobilization; a look ahead. Curr Stem Cell Rep. 2018;4:273–81.
  2. Indexed at, Google scholar

  3. West EE. Complement and human T cell metabolism: location, location, location. Immunol Rev. 2020;295:68–81.
  4. Indexed at, Google scholar, Cross ref

  5. Arbore G. Intracellular complement - the complosome - in immune cell regulation. Mol Immunol. 2017;89:2–9.
  6. Indexed at, Google scholar, Cross ref

  7. Rahman J. Complement’s favourite organelle-mitochondria? Br J Pharm. 2021;178:2771–85.
  8. Indexed at, Google scholar, Cross ref

  9. Kunz N. Complement has brains-do intracellular complement and immunometabolism cooperate in tissue homeostasis and behavior? Front Immunol. 2021;12:629986.
  10. Indexed at, Google scholar, Cross ref

Get the App