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I am a beginner in immune system. I am trying to understand the connection between T-Cell and Thymus as person ages.

It is clear from Guyton & Hall that till teenage the T-cell from bone marrow comes to Thymus which further gets filtered so that T-Cell does not attack self antigen (normal antigen of body). In this process of filtering out T-cells about 90% of the T-cells produced in bone marrow is destroyed in Thymus.

And then its said that, after teenage Thymus gets partially inactive OR it can be removed. Now what I am unable to understand is if Thymus gets removed/inactivated, in say a 45 year old person, who is going to filter the T-cells produced in bone marrow; by filtering I mean kill off the T-cells which can attack self-antigen of body.

If anyone can throw some light, it would be great.

User Afshar
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Final answer:

As individuals age, the thymus involutes and its efficiency in processing T cells declines, but memory T cells and peripheral tolerance mechanisms continue to ensure immune function. Regulatory T cells and other tolerance processes in peripheral tissues help control self-reactive cells, and some new T cells can still mature. Thymectomy in adults does not drastically reduce immune function but may affect response to new pathogens.

Step-by-step explanation:

Understanding T-Cell and Thymus Aging

The thymus is a primary lymphoid organ crucial for the maturation of T cells, which are vital components of the adaptive immune system. During childhood and adolescence, the thymus actively processes immature T cells, which originate from hematopoietic stem cells in the bone marrow. These T cells undergo two critical selection processes: positive selection, which ensures that T cells can recognise the body's own major histocompatibility complex (MHC) molecules, and negative selection, which eliminates T cells that strongly react with self-antigens. Consequently, the thymus plays a pivotal role in establishing T cell tolerance and preventing autoimmune responses.

As a person ages, the thymus begins to involute and its functionality declines. This is characterized by a decrease in thymic output of naive T cells, which can have implications for immune competence. However, the body does not become devoid of immune surveillance. T cells matured and educated in the thymus during the peak of its activity persist and form a pool of memory T cells. Additionally, peripheral tolerance mechanisms contribute to the control of self-reactive T cells after the thymus has involuted. These mechanisms include regulatory T cells (Tregs) that suppress autoimmune responses, anergy (unresponsiveness), and deletion of self-reactive T cells in peripheral tissues. Furthermore, new T cells can still mature to some extent, albeit less efficiently, as the thymus retains some function even after atrophy.

It is worth noting that while thymectomy (surgical removal of the thymus) in adults does not typically result in a dramatic loss of immune function, it can lead to a more rapid decline in the number of naive T cells, potentially impacting how the immune system responds to novel pathogens. Despite the reduced thymic function with age, the body maintains the capability to mount immune responses through the multiplicity of its immune surveillance strategies.

User Berimbolo
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