Commentary Article - (2022) Volume 30, Issue 5
Received: 02-May-2022, Manuscript No. IPQPC- 22-13526; Editor assigned: 03-May-2022, Pre QC No. IPQPC- 22-13526 (PQ); Reviewed: 18-May-2022, QC No. IPQPC- 22-13526; Revised: 23-May-2022, Manuscript No. IPQPC- 22-13526 (R); Published: 30-May-2022, DOI: 10.36648/1479-1072.22.30.47
Immunodeficiency deficiency, also called immunocompromisation, is a condition in which the immune system’s ability to fight off preventable diseases and malignant growths is compromised or completely absent. The conditions for such use are to move a member of the medical system as an enemy of expulsion and to patients with an overactive protective structure, such as in immune disorders. Some people are brought into the world with a natural defect in their immune system, or a significant deficiency in the immune system. A person with immunodeficiency of any kind should be immunocompromised. A person who is physically protected may not be able to resist commercial contamination, despite common ailments that can affect anyone. Addition weakens the immune system’s defenses, in which the invasive structure scans the body’s cells and kills neoplastic cells. In addition they are at greater risk of undiagnosed diseases due to decreased certainty controlled by the immune system. Humoral deficiency (counting deficiency or B cell fractures), and symptoms or side effects depending on the cause, however often include symptoms of hypogammaglobulinemia (reduction of at least one type of immune system) and presentations that include recurrent respiratory infections, or possibly agammaglobulinemia (the absence of it all or the formation of a mass vaccine) which brings about serious continuous and often deadly pollution. Lack of white blood cells, often causes your own choices such as AIDS (AIDS). Granulocyte deficiency, which includes reduced levels of granulocyte (called granulocytopenia or vice versa, agranulocytosis, for example, neutrophil granulocytes (called neutropenia). Deficiency of the supplement is where the strength of the draft ingredient is lacking. The reduced capacity of a non-invasive framework to remove impurities from these patients may be responsible for autoimmune immunity by the establishment of a permanent safe framework. Appear, e.g., sexually transmitted infections, immune system thrombocytopenia, and thyroid disease. Familial hemophagocytic lymphohistiocytosis, autosomal passive essential immunodeficiency, is another example. Low blood levels of red platelets, white platelets, and platelets, rash, lymph hub amplification, and enlarged liver and spleen are commonly found in these patients. The presence of various subtle contaminants due to the lack of performing is believed to be possible. Despite persistent infection and occasional exacerbation of many autoimmune diseases including joint pain, immune system hemolytic pallor, scleroderma and type 1 diabetes are also found in X-connected agammaglobulinemia (XLA). Repeated contamination caused by viruses and infections as well as progressive irritation of the stomach and lungs is reflected in the progressive granulomatous infection (CGD). CGD is caused by a decrease in the production of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase by neutrophils.
Hypomorphic RAG mutations are found in patients with midline granulomatous disease; an autoimmune disorder commonly found in patients with granulomatosis with polyangiitis and NK / T cell lymphomas. Wiskott-Aldrich condition (WAS) patients also have dermatitis, symptoms of an immune system, occasional contamination and lymphoma. In the immune system polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in addition immunosuppression and disease are present together: indications of a clear immune system and progressive mucocutaneous candidiasis. Finally, IgA deficiency is also sometimes associated with the development of immune and atopic factors.
The author is grateful to the journal editor and the anonymous reviewers for their helpful comments and suggestions.
The author declared no potential conflicts of interest for the research, authorship, and/or publication of this article.
Citation: Lucas J (2022) Effect of Immunodeficiency and It Causes. Qual Prim Care. 30.41814.
Copyright: © Lucas J. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
