Why is there an extended delay before G.M. liver cells are attacked by the immune system?
There can be several factors that contribute to the extended delay before G.M. (genetically modified) liver cells are attacked by the immune system. Here are a few possible reasons:
1. Reduced recognition by the immune system: Genetic modification can lead to changes in the surface proteins on the G.M. liver cells. These modified proteins may not be recognized as foreign by the immune system, causing a delay in immune response. The immune system typically relies on recognizing foreign antigens on cells to trigger an immune response.
2. Suppression of immune response: It is possible that the genetic modifications in the liver cells may affect the production or release of certain molecules that suppress the immune response. These molecules, such as immunosuppressive cytokines, can dampen the activity of immune cells, prolonging the time before the immune system launches an attack.
3. Lower immunogenicity: Genetic modifications in liver cells could result in reduced immunogenicity, meaning they may not provoke a strong immune response. This could be due to changes in the expression of major histocompatibility complex (MHC) molecules, which present antigens to immune cells. If the modified liver cells have altered MHC expression, they may be less likely to be recognized and attacked by immune cells.
4. Tolerance induction: The liver has unique immunological properties that can induce a state of immunological tolerance, which prevents the immune system from launching an aggressive response against its own cells. This is beneficial to maintain liver function, but it may also contribute to the delay in immune system recognition of genetically modified liver cells.
5. Immune privilege: Some tissues in the body, including the liver, are considered immunologically privileged sites. This means they have mechanisms that limit immune cell infiltration and activation. The liver, being responsible for detoxification and metabolism, has evolved mechanisms to prevent immune-mediated damage. These mechanisms could delay the immune response to genetically modified liver cells.
It is important to note that the dynamics of the immune response to genetically modified liver cells can vary depending on the specific genetic modifications and the individual’s immune system. The immune response is a complex and highly regulated process, and further research is necessary to fully understand the precise mechanisms underlying the extended delay before immune attack on G.M. liver cells.
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