Opinion Article - Research and Reports in Immunology (2023) Volume 6, Issue 3
Immune cells defenders of the body's fortress
Manish Muhuri*Department of Immunology, University of Washington, Seattle, Washington
- *Corresponding Author:
- Manish Muhuri
Department of Immunology
University of Washington, Seattle, Washington
E-mail: Sarahanderson@gmail.com
Received: 31-Mar-2023, Manuscript No. AARRI-23-97312; Editor assigned: 03-Apr-2023, Pre QC No. AARRI-23-97312(PQ); Reviewed: 17-Apr-2023, QC No. AARRI-23-97312; Revised: 22-Apr-2023, Manuscript No. AARRI -23-97312(R); Published: 29-Apr-2023, DOI: 10.35841/aarri-6.2.145
Citation: Muhuri M. Immune cells defenders of the body's fortress. Res Rep Immunol. 2023; 6(3):146
Introduction
Phagocytes, including neutrophils and macrophages, are the body's first line of defense against invading pathogens. These cells specialize in engulfing and destroying foreign substances such as bacteria, viruses, and dead cells. Neutrophils are the most abundant type of white blood cell and are swiftly deployed to sites of infection. Macrophages, on the other hand, act as scavengers, cleaning up debris and initiating the immune response. Lymphocytes are a key component of the adaptive immune system, which provides long-term immunity against specific pathogens [1,2]. There are two main types of lymphocytes: B cells and T cells. B cells produce antibodies that neutralize harmful substances, while T cells identify and destroy infected cells. Within the T cell population, helper T cells coordinate immune responses, while killer T cells directly attack infected or cancerous cells. Natural Killer cells are a unique type of immune cell that can detect and eliminate virus-infected cells and tumor cells without prior exposure. These cells play a crucial role in the early stages of the immune response, bridging the gap between the innate and adaptive immune systems. Dendritic cells act as messengers between the innate and adaptive immune systems. They capture antigens, molecules that trigger immune responses, and present them to other immune cells, such as T cells. This presentation allows the adaptive immune system to mount a specific and targeted response against the invading pathogen [3].
Immune cells possess specialized receptors that recognize specific molecules associated with pathogens. These receptors enable the immune cells to detect the presence of harmful invaders and initiate an appropriate response. Upon detection, immune cells release chemical signals called cytokines, which act as alarm bells, alerting other immune cells to the presence of a threat. This coordination leads to an orchestrated immune response, activating various cells and mechanisms to combat the pathogen [4].
Certain immune cells, such as macrophages, neutrophils, and killer T cells, engage in direct confrontation with pathogens. They engulf and destroy pathogens or infected cells, preventing the spread of infection within the body. B cells are responsible for producing antibodies, which are proteins that recognize and bind to specific pathogens. Antibodies neutralize pathogens, mark them for destruction by other immune cells, and enhance the effectiveness of the immune response. One of the most remarkable aspects of the immune system is its ability to "remember" previous encounters with pathogens. Memory B cells and memory T cells retain information about specific pathogens, allowing for a rapid and robust immune response upon subsequent exposure. This memory provides long-term protection against reinfection [5].
Conclusion
Immune cells are the unsung heroes of our bodies, tirelessly working to protect us from harm. From phagocytes to lymphocytes, each type of immune cell has a unique role in detecting, neutralizing, and eliminating pathogens. Through their coordination, immune cells mount complex responses that shield us from infections.
References
- Wainberg MA. Development of antiretroviral drug resistance. N Engl J Med.2011; 365:637–46.
- Mesplede T. Resistance against integrase strand transfer inhibitors and relevance to HIV persistence. Viruses 7:3703–18.
- Borden EC. Interferons at age 50: past, current and future impact on biomedicine. Nat Rev Drug Discov.2007;6:975–90.
- Haller O. Mx GTPases: dynamin-like antiviral machines of innate immunity. Trends Microbiol. 2015; 23:154–63.
- Verhelst J. Mx proteins: antiviral gatekeepers that restrain the uninvited. Microbiol Mol Biol Rev. 2013; 77:551–66.
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