Viruses can use various mechanisms to evade the immune system, including molecular mimicry, antigenic shift, and latency. Molecular mimicry involves the virus mimicking host molecules to avoid recognition by the immune system. Antigenic shift refers to the ability of some viruses to change their surface proteins, making them unrecognizable to the immune system. Latency is a state in which the virus remains dormant within the host, evading immune detection.

Viral glycoproteins play a crucial role in the initial attachment of the virus to host cells, facilitating viral entry and infection. They are not primarily involved in immune recognition and neutralization, viral replication, or assembly.

Influenza virus is a well-known example of a virus that undergoes antigenic shift. This process involves the reassortment of viral RNA segments, leading to the emergence of new viral strains with altered surface proteins. This allows the virus to evade pre-existing immunity and cause recurrent infections.

HIV employs multiple strategies to evade the immune system, including targeting CD4+ T cells. The virus expresses viral proteins that inhibit the function of CD4+ T cells, downregulates the expression of MHC class II molecules on infected cells, and induces apoptosis of CD4+ T cells. These mechanisms contribute to the depletion of CD4+ T cells and the development of AIDS.

Latency is a state in which the virus remains dormant within the host, evading immune detection. This allows the virus to persist in the host for extended periods without causing overt disease. During latency, the virus can prevent the immune system from recognizing and eliminating infected cells, and it can also facilitate the spread of the virus to new host cells.

Herpes simplex virus (HSV) is an example of a virus that establishes latency. After the initial infection, HSV can enter a latent state in sensory nerve ganglia. During latency, the virus remains dormant and evades the immune system. However, it can reactivate under certain conditions, leading to recurrent infections.

Molecular mimicry is a mechanism by which viruses evade the immune system by mimicking host molecules. This allows the virus to escape recognition by the immune system, interfere with the function of immune cells, and promote the survival of infected cells. Molecular mimicry can involve the imitation of host proteins, carbohydrates, or even MHC molecules.

Hepatitis B virus (HBV), human immunodeficiency virus (HIV), and cytomegalovirus (CMV) are all examples of viruses that use molecular mimicry to evade the immune system. HBV mimics host proteins to avoid recognition by the immune system. HIV mimics MHC molecules to interfere with the function of immune cells. CMV mimics host proteins to promote the survival of infected cells.

Viral interference is a phenomenon in which the replication of one virus in a cell prevents the replication of other viruses. This can occur through various mechanisms, such as the production of antiviral proteins, the degradation of viral RNA or DNA, or the inhibition of viral entry or assembly. By preventing the replication of other viruses, viral interference can contribute to the survival of the infecting virus and evade the immune system.

Herpes simplex virus (HSV) is an example of a virus that uses viral interference to evade the immune system. HSV can produce antiviral proteins that inhibit the replication of other viruses in infected cells. This can help HSV to establish and maintain latency, as well as to prevent superinfection by other viruses.

Viral mutations can contribute to immune evasion in several ways. They can lead to the emergence of new viral strains that are unrecognizable to the immune system, alter the structure of viral proteins, making them less susceptible to immune recognition, and disrupt the function of viral proteins that are involved in immune evasion. These mutations can help the virus to escape immune surveillance and establish persistent infections.

Influenza virus, human immunodeficiency virus (HIV), and hepatitis C virus (HCV) are all examples of viruses that use viral mutations to evade the immune system. Influenza virus undergoes antigenic drift, which involves the accumulation of point mutations in the viral genome, leading to the emergence of new viral strains that are unrecognizable to the immune system. HIV and HCV have high mutation rates, which allow them to rapidly generate new variants that can escape immune recognition.

Viral shedding contributes to immune evasion by releasing large amounts of virus particles into the environment, overwhelming the immune system with a high viral load, and facilitating the transmission of the virus to new hosts. By shedding large amounts of virus, the virus can increase its chances of infecting new cells and establishing new infections. The high viral load can overwhelm the immune system, making it difficult to control the infection. Additionally, viral shedding can facilitate the transmission of the virus to new hosts, allowing the virus to spread and evade immune responses in new populations.

Influenza virus, measles virus, and varicella-zoster virus (VZV) are all examples of viruses that use viral shedding to evade the immune system. Influenza virus is shed in respiratory droplets when an infected person coughs or sneezes. Measles virus is shed in respiratory droplets and urine. VZV is shed in skin lesions and respiratory droplets. Viral shedding by these viruses facilitates their transmission to new hosts and contributes to their ability to evade immune responses.

Immune suppression plays a crucial role in viral immune evasion by weakening the immune response to the virus, preventing the development of memory immune responses, and facilitating the establishment of persistent infections. By suppressing the immune system, the virus can evade immune detection and elimination, allowing it to persist in the host for extended periods. Immune suppression can be caused by various viral proteins, such as those that inhibit the function of immune cells or interfere with immune signaling pathways.

Human immunodeficiency virus (HIV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV) are all examples of viruses that use immune suppression to evade the immune system. HIV infects and destroys CD4+ T cells, leading to severe immune suppression. CMV and EBV can also suppress the immune system by expressing viral proteins that interfere with immune cell function or signaling pathways.