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Ch. 16 - Innate Immunity: Nonspecific Defenses of the Host
Chapter 12, Problem 16.7a

Give several examples of how microbes evade the complement system.

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Identify the role of the complement system in the immune response, which includes opsonization, inflammation, and lysis of pathogens.
Understand that microbes have evolved various strategies to evade the complement system to survive and cause infection.
Explore how some bacteria produce proteins that bind to complement proteins, preventing their activation or function.
Examine how certain pathogens can mimic host cell surfaces to avoid detection and attack by the complement system.
Investigate how some microbes secrete enzymes that degrade complement proteins, thereby neutralizing their effects.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Complement System

The complement system is a part of the immune system that enhances the ability to clear pathogens from an organism. It consists of a series of proteins that, when activated, can opsonize pathogens, recruit inflammatory cells, and directly lyse microbes. Understanding how this system functions is crucial for comprehending how microbes can develop strategies to evade it.
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Microbial Evasion Strategies

Microbes have evolved various strategies to evade the complement system, including the production of surface proteins that inhibit complement activation or binding. Some bacteria can also modify their surface structures, such as polysaccharide capsules, to prevent opsonization. These evasion tactics allow pathogens to survive and proliferate despite the host's immune responses.
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Pathogen-Host Interactions

Pathogen-host interactions refer to the dynamic relationship between invading microbes and the host's immune system. Understanding these interactions is essential for identifying how pathogens exploit weaknesses in the immune response, including the complement system. This knowledge can inform the development of therapeutic strategies and vaccines to enhance host defenses against infections.
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