The main functions of the immune system include protecting from _______ and playing a role in many aspects of _______.
The main functions of the immune system include protecting from infection and playing a role in many aspects of health and disease.
The two major arms of the immune response are _______ and _______.
The two major arms of the immune response are innate immunity and adaptive immunity.
The innate immune system responds rapidly using _______ that recognize broad classes of _______.
The innate immune system responds rapidly using germline encoded immune receptors that recognize broad classes of pathogens.
The adaptive immune system responds more slowly but with higher _______ and has memory capabilities.
The adaptive immune system responds more slowly but with higher specificity and has memory capabilities.
The major cell types of innate immunity include _______, _______, and _______.
The major cell types of innate immunity include macrophages, neutrophils, and natural killer cells.
The major cell types of adaptive immunity include _______ and _______.
The major cell types of adaptive immunity include T cells and B cells.
Cellular immunity primarily removes _______ while humoral immunity targets _______.
Cellular immunity primarily removes intracellular pathogens while humoral immunity targets extracellular pathogens.
Cluster of differentiation (CD) markers are used to identify specific _______ in the immune system, such as _______ for T helper cells and _______ for cytotoxic T cells.
Cluster of differentiation (CD) markers are used to identify specific cell types in the immune system, such as CD4 for T helper cells and CD8 for cytotoxic T cells.
The immune system distinguishes _______ from _______ using innate and adaptive immune responses.
The immune system distinguishes self from non-self using innate and adaptive immune responses.
The primary role of the immune system is to protect from _______ and also to defend against _______.
The primary role of the immune system is to protect from infection and also to defend against tumors.
Inappropriate immune responses can lead to conditions such as _______ and allergies.
Inappropriate immune responses can lead to conditions such as autoimmunity and allergies.
The immune system plays a role in tissue _______ and _______.
The immune system plays a role in tissue regeneration and scarring.
A successful immune response includes features such as _______, _______, and _______.
A successful immune response includes features such as recognition of pathogens, activation of immune cells, and elimination of pathogens.
The immune response to a pathogen involves the following steps: 1) _______ of a pathogen; 2) Determining the _______ of pathogen; 3) _______ of the pathogen; 4) Development of _______; and 5) Avoiding damage to _______.
The immune response to a pathogen involves the following steps: 1) Recognition of a pathogen; 2) Determining the type of pathogen; 3) Elimination of the pathogen; 4) Development of immune memory; and 5) Avoiding damage to self-tissues.
The immune system must defend the body from infection while maintaining tolerance to _______ and to _______.
The immune system must defend the body from infection while maintaining tolerance to self and to commensal organisms.
The immune system is organized into two major arms: the _______ and the _______.
The immune system is organized into two major arms: the innate immune response and the adaptive immune response.
Key cell types of the _______ include _______, _______, and others such as _______ and _______.
Key cell types of the innate immune response include myeloid cells, natural killer cells, and others such as macrophages and neutrophils.
The adaptive immune response is characterized by _______ and _______.
The adaptive immune response is characterized by B and T lymphocytes.
B lymphocytes produce _______ that block infection and eliminate _______.
B lymphocytes produce antibodies that block infection and eliminate extracellular pathogens.
T lymphocytes are responsible for eradicating _______.
T lymphocytes are responsible for eradicating intracellular pathogens.
Innate immunity includes immediate defense mechanisms such as _______, _______, and _______.
Innate immunity includes immediate defense mechanisms such as mechanical barriers, chemical barriers, and biological barriers.
The innate immune system recognizes broad categories of pathogens through germline-encoded innate immune _______.
The innate immune system recognizes broad categories of pathogens through germline-encoded innate immune receptors.
Adaptive immunity generates _______ immunity through specialized antigen receptors on _______.
Adaptive immunity generates pathogen-specific immunity through specialized antigen receptors on lymphocytes.
The specialized antigen receptors of B lymphocytes can be secreted as _______.
The specialized antigen receptors of B lymphocytes can be secreted as antibodies.
The diagram illustrates the principal components of innate and adaptive immunity over time after infection, showing that innate immunity acts within _______ while adaptive immunity develops over _______. 
The diagram illustrates the principal components of innate and adaptive immunity over time after infection, showing that innate immunity acts within hours while adaptive immunity develops over days. 
The innate immune response includes cells such as _______ and _______.
The innate immune response includes cells such as phagocytes and NK cells.
Mechanical barriers in innate immunity include _______ and _______.
Mechanical barriers in innate immunity include skin and mucus.
Chemical barriers in innate immunity include enzymes like _______ and antimicrobial proteins such as _______.
Chemical barriers in innate immunity include enzymes like lysozyme and antimicrobial proteins such as beta-defensins.
The process of recognizing a pathogen in the immune response is known as _______.
The process of recognizing a pathogen in the immune response is known as pathogen recognition.
The elimination of a pathogen involves determining the _______.
The elimination of a pathogen involves determining the appropriate response.
The development of immune memory leads to a _______ and more _______ upon re-exposure to the same pathogen.
The development of immune memory leads to a faster and more robust response upon re-exposure to the same pathogen.
The receptor of T lymphocytes is the _______.
The receptor of T lymphocytes is the T cell receptor.
Humoral immunity involves _______ that secrete _______ to eliminate extracellular microbes.
Humoral immunity involves B lymphocytes that secrete antibodies to eliminate extracellular microbes.
Cell-mediated immunity involves _______ that can kill infected cells and eliminate reservoirs of infection.
Cell-mediated immunity involves T lymphocytes that can kill infected cells and eliminate reservoirs of infection.
The adaptive immune response has a noticeable _______ to initiation, beginning _______ after pathogen exposure.
The adaptive immune response has a noticeable lag phase to initiation, beginning four to seven days after pathogen exposure.
Adaptive immune responses are highly _______ and have _______ for quicker defense upon re-exposure to the same pathogen.
Adaptive immune responses are highly antigen-specific and have memory capabilities for quicker defense upon re-exposure to the same pathogen.
Innate immune cells do not have the same _______ as adaptive immune cells.
Innate immune cells do not have the same memory capability as adaptive immune cells.
In humoral immunity, B lymphocytes secrete _______ that eliminate _______.
In humoral immunity, B lymphocytes secrete antibodies that eliminate extracellular microbes.
In cell-mediated immunity, some T lymphocytes secrete _______ that recruit and activate _______.
In cell-mediated immunity, some T lymphocytes secrete cytokines that recruit and activate phagocytes.
Cytotoxic T lymphocytes (CTLs) kill _______ and eliminate reservoirs of _______.
Cytotoxic T lymphocytes (CTLs) kill infected cells and eliminate reservoirs of infection.
Phagocytes can ingest and destroy pathogens such as _______ and _______.
Phagocytes can ingest and destroy pathogens such as Borrelia burgdorferi and Salmonella typhi.
Humoral immunity refers to soluble substances found in _______ and other body _______.
Humoral immunity refers to soluble substances found in blood and other body fluids.
Antibodies secreted by B lymphocytes bind to microbes, preventing further _______ and enhancing microbial uptake by _______.
Antibodies secreted by B lymphocytes bind to microbes, preventing further dissemination and enhancing microbial uptake by phagocytes.
The immune system uses both _______ and _______ to defend the body.
The immune system uses both cells and secreted factors to defend the body.
Cellular immunity refers to _______, while humoral immunity refers to soluble immune factors like _______.
Cellular immunity refers to cells, while humoral immunity refers to soluble immune factors like antibodies.
The immune mechanisms that effectively clear _______ may not be the same as those effective against _______.
The immune mechanisms that effectively clear Borrelia burgdorferi may not be the same as those effective against Salmonella typhi.
Phagocytes can ingest and destroy pathogens they encounter in _______.
Phagocytes can ingest and destroy pathogens they encounter in body fluids.
The comparison of humoral and cell-mediated immunity shows that humoral immunity involves _______ and secreted _______, while cell-mediated immunity involves _______ and _______.
The comparison of humoral and cell-mediated immunity shows that humoral immunity involves B lymphocytes and secreted antibodies, while cell-mediated immunity involves T lymphocytes and macrophages.
The principal function of _______ is to engulf pathogens and present digested pieces to alert and recruit other immune cells. Examples of APCs include _______, _______, and _______.
The principal function of antigen presenting cells (APCs) is to engulf pathogens and present digested pieces to alert and recruit other immune cells. Examples of APCs include macrophages, B cells, and dendritic cells.
_______ include B and T cells, which mediate specific recognition of pathogens. Upon encountering their specific antigen, they undergo _______ and differentiate into specialized subtypes such as _______ and _______.
Antigen-specific lymphocytes include B and T cells, which mediate specific recognition of pathogens. Upon encountering their specific antigen, they undergo clonal proliferation and differentiate into specialized subtypes such as effector cells and memory cells.
Effector cells carry out the functions of the immune response and include _______, _______, and _______. These cells can mediate the removal of pathogens without further differentiation.
Effector cells carry out the functions of the immune response and include macrophages, granulocytes, and T cells. These cells can mediate the removal of pathogens without further differentiation.
B lymphocytes are mediators of _______, while T lymphocytes are mediators of _______.
B lymphocytes are mediators of humoral immunity, while T lymphocytes are mediators of cell-mediated immunity.
Dendritic cells initiate _______, while macrophages are involved in the _______ of cell-mediated immunity.
Dendritic cells initiate T cell responses, while macrophages are involved in the effector phase of cell-mediated immunity.
_______ include neutrophils, basophils, and eosinophils, which phagocytose pathogens and mediate inflammation.
Granulocytes include neutrophils, basophils, and eosinophils, which phagocytose pathogens and mediate inflammation.
Mast cells regulate blood vessel dilation and mediate _______.
Mast cells regulate blood vessel dilation and mediate inflammation.
_______ destroy virally infected or tumorigenic cells as part of the innate immune response.
Natural Killer (NK) cells destroy virally infected or tumorigenic cells as part of the innate immune response.
B lymphocytes produce _______ (immunoglobulins) that are specialized for each pathogen and found in the blood as soluble proteins.
B lymphocytes produce antibodies (immunoglobulins) that are specialized for each pathogen and found in the blood as soluble proteins.
T lymphocytes recognize infected or transformed cells and are responsible for their _______ and elimination from the body.
T lymphocytes recognize infected or transformed cells and are responsible for their destruction and elimination from the body.
The table detailing cell types and their principal functions in the immune system includes lymphocytes (B and T cells), antigen-presenting cells (dendritic cells, macrophages), and effector cells (T lymphocytes, macrophages, granulocytes). See image: 
The table detailing cell types and their principal functions in the immune system includes lymphocytes (B and T cells), antigen-presenting cells (dendritic cells, macrophages), and effector cells (T lymphocytes, macrophages, granulocytes). See image: 
Immune cells can be identified by their cell surface molecules called _______. These are receptors or proteins found on the _______.
Immune cells can be identified by their cell surface molecules called CD Markers. These are receptors or proteins found on the plasma membrane.
All B lymphocytes express the cell surface receptors _______ and _______.
All B lymphocytes express the cell surface receptors CD19 and CD20.
All T cells express _______.
All T cells express CD3.
CD3+ T cells can be divided into two subsets: _______ and _______.
CD3+ T cells can be divided into two subsets: CD4 helper T cells and CD8 cytotoxic T cells.
CD4 helper T cells provide help signals to activate other immune subsets, while CD8 cytotoxic T cells _______.
CD4 helper T cells provide help signals to activate other immune subsets, while CD8 cytotoxic T cells kill infected or cancerous cells.
Clinical diagnostics use the CD marker system to identify a patient's type of _______ or _______ cell.
Clinical diagnostics use the CD marker system to identify a patient's type of leukemia or lymphoma cell.
Major identifying cell surface markers for immune cells include CD34 and c-kit for _______.
Major identifying cell surface markers for immune cells include CD34 and c-kit for Hematopoietic stem cells (HSC).
B cells express the surface markers _______ and _______.
B cells express the surface markers CD19 and CD20.
T cells express the surface marker _______.
T cells express the surface marker CD3.
NK cells express the surface markers _______ and _______.
NK cells express the surface markers CD16 and CD56.
Antigens are defined as an organism, molecule, or part of a molecule that is recognized by the _______.
Antigens are defined as an organism, molecule, or part of a molecule that is recognized by the immune system.
Antigens can be simple or complex, protein or _______.
Antigens can be simple or complex, protein or carbohydrate.
The immune system can recognize _______, which refers to changes in the body's cells after infection or malignant transformation.
The immune system can recognize altered self, which refers to changes in the body's cells after infection or malignant transformation.
Altered self antigens may be _______ or normal proteins expressed at higher levels due to aberrant regulation.
Altered self antigens may be mutated gene products or normal proteins expressed at higher levels due to aberrant regulation.
Microorganisms bear repeating patterns of molecular structure on their surface, known as _______ or _______.
Microorganisms bear repeating patterns of molecular structure on their surface, known as PAMPs or DAMPs.
PAMPs are specific targets of the immune system and include structures like the cell walls of _______ and _______ bacteria.
PAMPs are specific targets of the immune system and include structures like the cell walls of Gram-positive and Gram-negative bacteria.
Bacterial flagella are made up of _______.
Bacterial flagella are made up of repetitive protein subunits.
Many viruses express _______ as part of their life cycle.
Many viruses express double-stranded RNA as part of their life cycle.
Innate immune cells use receptors that are _______ to recognize pathogen-associated antigens.
Innate immune cells use receptors that are germline encoded to recognize pathogen-associated antigens.
B and T cells express receptors generated through _______.
B and T cells express receptors generated through DNA recombination.
The process of DNA rearrangement can generate up to _______} unique receptors.
The process of DNA rearrangement can generate up to 10^{17} unique receptors.
Each B or T cell expresses only one type of receptor, which is always on the cell surface, although B cells can secrete their receptors in the form of _______.
Each B or T cell expresses only one type of receptor, which is always on the cell surface, although B cells can secrete their receptors in the form of antibodies.
Illustration shows an _______ with antibodies bound to its surface. 
Illustration shows an antigen with antibodies bound to its surface. 
Table listing major identifying cell surface markers includes Hematopoietic stem cell, B cell, T cell, and NK cell with their corresponding _______. 
Table listing major identifying cell surface markers includes Hematopoietic stem cell, B cell, T cell, and NK cell with their corresponding CD markers. 
The two main types of immunity are _______ and _______.
The two main types of immunity are innate immunity and adaptive immunity.
Innate immunity recognizes structures shared by classes of microbes known as _______.
Innate immunity recognizes structures shared by classes of microbes known as PAMPs.
Adaptive immunity recognizes specific structural details of microbial molecules called _______.
Adaptive immunity recognizes specific structural details of microbial molecules called antigens.
The receptors used in innate immunity are located in the _______, _______, and _______.
The receptors used in innate immunity are located in the plasma membrane, endosomal membrane, and cytosol.
The receptors in adaptive immunity are located only in the _______.
The receptors in adaptive immunity are located only in the plasma membrane.
Innate immunity has about _______ different types of invariant receptors, while adaptive immunity has only _______ types of receptors (Ig and TCR).
Innate immunity has about 100 different types of invariant receptors, while adaptive immunity has only 2 types of receptors (Ig and TCR).
The number of unique antigens recognized by the adaptive immune system is estimated to be greater than _______.
The number of unique antigens recognized by the adaptive immune system is estimated to be greater than 10^7.
In the immune response, clonal expansion can lead to about _______ microbe-specific T cells.
In the immune response, clonal expansion can lead to about 10^6 microbe-specific T cells.
The contraction phase of the immune response results in about _______ T cells remaining after the response.
The contraction phase of the immune response results in about 10^4 T cells remaining after the response.
The early innate defense relies on invariant, germline-encoded receptors recognizing common features of _______.
The early innate defense relies on invariant, germline-encoded receptors recognizing common features of pathogens.
Adaptive immunity provides enhanced protection against reinfection by recognizing a particular _______.
Adaptive immunity provides enhanced protection against reinfection by recognizing a particular pathogen.
The classic cadence of the immune response shows the number of microbe-specific T cells over time, indicating phases of _______ and _______.
The classic cadence of the immune response shows the number of microbe-specific T cells over time, indicating phases of clonal expansion and contraction.
The graph depicting the classic cadence of the immune response shows the number of CD8+ T cells and CD4+ T cells over _______.
The graph depicting the classic cadence of the immune response shows the number of CD8+ T cells and CD4+ T cells over days after infection.
The innate immune system is crucially important but has limitations as it can be overcome by many _______.
The innate immune system is crucially important but has limitations as it can be overcome by many pathogens.
Adaptive immunity is characterized by the formation of _______ after an initial response to a pathogen.
Adaptive immunity is characterized by the formation of memory cells after an initial response to a pathogen.
The discrimination of self and nonself in innate immunity is based on the recognition of healthy host cells that do not express certain _______.
The discrimination of self and nonself in innate immunity is based on the recognition of healthy host cells that do not express certain molecules.
In adaptive immunity, self-reactive lymphocytes are eliminated or inactivated to avoid _______.
In adaptive immunity, self-reactive lymphocytes are eliminated or inactivated to avoid autoimmunity.
The genes encoding receptors in innate immunity are _______ and present in all cells.
The genes encoding receptors in innate immunity are germline encoded and present in all cells.
In adaptive immunity, receptors are formed by _______ of gene segments only in B and T cells.
In adaptive immunity, receptors are formed by somatic recombination of gene segments only in B and T cells.
The table comparing innate and adaptive immunity features highlights differences in specificity, microbial molecules recognized, receptors, distribution, genes, and self-non-self discrimination. See the comparison table for details: 
The table comparing innate and adaptive immunity features highlights differences in specificity, microbial molecules recognized, receptors, distribution, genes, and self-non-self discrimination. See the comparison table for details: 
The innate immune response fails to eliminate a new infection, leading to activated _______ being delivered to the _______.
The innate immune response fails to eliminate a new infection, leading to activated antigen presenting cells being delivered to the draining lymph nodes.
When a recirculating lymphocyte encounters its corresponding _______, it is induced to proliferate and differentiate into _______.
When a recirculating lymphocyte encounters its corresponding antigen, it is induced to proliferate and differentiate into effector B or T lymphocytes.
A subset of proliferating lymphocytes differentiates into _______, which are ready to respond rapidly to the same pathogen if encountered again.
A subset of proliferating lymphocytes differentiates into memory cells, which are ready to respond rapidly to the same pathogen if encountered again.
After infection clears, antigen-specific lymphocytes gradually decrease from its peak in a phase called _______.
After infection clears, antigen-specific lymphocytes gradually decrease from its peak in a phase called resolution phase.
Following resolution, antigen-specific lymphocytes are sustained at a level that is slightly _______ than prior to infection, contributing to _______.
Following resolution, antigen-specific lymphocytes are sustained at a level that is slightly higher than prior to infection, contributing to immunological memory.
The immune system defends the body against infection, with the innate immune system acting quickly but lacking the ability to recognize certain _______.
The immune system defends the body against infection, with the innate immune system acting quickly but lacking the ability to recognize certain pathogens.
Adaptive immunity is based on _______ from a repertoire of lymphocytes bearing highly diverse _______.
Adaptive immunity is based on clonal selection from a repertoire of lymphocytes bearing highly diverse antigen-specific receptors.
Host defense requires different recognition systems and a wide variety of _______ to seek out and destroy diverse pathogens.
Host defense requires different recognition systems and a wide variety of effector mechanisms to seek out and destroy diverse pathogens.
The innate immune system provides _______ protective immunity, while adaptive immunity provides _______ protective immunity that prevents reinfection.
The innate immune system provides non-specific protective immunity, while adaptive immunity provides specific protective immunity that prevents reinfection.
The main functions of the immune system include protecting from infection and playing a role in many aspects of health and disease.
The innate immune system responds rapidly using germline encoded immune receptors that recognize broad classes of pathogens.
The adaptive immune system responds more slowly but with higher specificity and has memory capabilities.
Cellular immunity primarily removes intracellular pathogens while humoral immunity targets extracellular pathogens.
Cluster of differentiation (CD) markers are used to identify specific cell types in the immune system, such as CD4 for T helper cells and CD8 for cytotoxic T cells.
The primary role of the immune system is to protect from infection and also to defend against tumors.
A successful immune response includes features such as recognition of pathogens, activation of immune cells, and elimination of pathogens.
The immune response to a pathogen involves the following steps: 1) Recognition of a pathogen; 2) Determining the type of pathogen; 3) Elimination of the pathogen; 4) Development of immune memory; and 5) Avoiding damage to self-tissues.
The immune system must defend the body from infection while maintaining tolerance to self and to commensal organisms.
The immune system is organized into two major arms: the innate immune response and the adaptive immune response.
Key cell types of the innate immune response include myeloid cells, natural killer cells, and others such as macrophages and neutrophils.
Innate immunity includes immediate defense mechanisms such as mechanical barriers, chemical barriers, and biological barriers.
The innate immune system recognizes broad categories of pathogens through germline-encoded innate immune receptors.
Adaptive immunity generates pathogen-specific immunity through specialized antigen receptors on lymphocytes.
The diagram illustrates the principal components of innate and adaptive immunity over time after infection, showing that innate immunity acts within hours while adaptive immunity develops over days. 
Chemical barriers in innate immunity include enzymes like lysozyme and antimicrobial proteins such as beta-defensins.
The development of immune memory leads to a faster and more robust response upon re-exposure to the same pathogen.
Humoral immunity involves B lymphocytes that secrete antibodies to eliminate extracellular microbes.
Cell-mediated immunity involves T lymphocytes that can kill infected cells and eliminate reservoirs of infection.
The adaptive immune response has a noticeable lag phase to initiation, beginning four to seven days after pathogen exposure.
Adaptive immune responses are highly antigen-specific and have memory capabilities for quicker defense upon re-exposure to the same pathogen.
In cell-mediated immunity, some T lymphocytes secrete cytokines that recruit and activate phagocytes.
Antibodies secreted by B lymphocytes bind to microbes, preventing further dissemination and enhancing microbial uptake by phagocytes.
Cellular immunity refers to cells, while humoral immunity refers to soluble immune factors like antibodies.
The immune mechanisms that effectively clear Borrelia burgdorferi may not be the same as those effective against Salmonella typhi.
The comparison of humoral and cell-mediated immunity shows that humoral immunity involves B lymphocytes and secreted antibodies, while cell-mediated immunity involves T lymphocytes and macrophages.
The principal function of antigen presenting cells (APCs) is to engulf pathogens and present digested pieces to alert and recruit other immune cells. Examples of APCs include macrophages, B cells, and dendritic cells.
Antigen-specific lymphocytes include B and T cells, which mediate specific recognition of pathogens. Upon encountering their specific antigen, they undergo clonal proliferation and differentiate into specialized subtypes such as effector cells and memory cells.
Effector cells carry out the functions of the immune response and include macrophages, granulocytes, and T cells. These cells can mediate the removal of pathogens without further differentiation.
B lymphocytes are mediators of humoral immunity, while T lymphocytes are mediators of cell-mediated immunity.
Dendritic cells initiate T cell responses, while macrophages are involved in the effector phase of cell-mediated immunity.
Granulocytes include neutrophils, basophils, and eosinophils, which phagocytose pathogens and mediate inflammation.
Natural Killer (NK) cells destroy virally infected or tumorigenic cells as part of the innate immune response.
B lymphocytes produce antibodies (immunoglobulins) that are specialized for each pathogen and found in the blood as soluble proteins.
T lymphocytes recognize infected or transformed cells and are responsible for their destruction and elimination from the body.
The table detailing cell types and their principal functions in the immune system includes lymphocytes (B and T cells), antigen-presenting cells (dendritic cells, macrophages), and effector cells (T lymphocytes, macrophages, granulocytes). See image: 
Immune cells can be identified by their cell surface molecules called CD Markers. These are receptors or proteins found on the plasma membrane.
CD4 helper T cells provide help signals to activate other immune subsets, while CD8 cytotoxic T cells kill infected or cancerous cells.
Clinical diagnostics use the CD marker system to identify a patient's type of leukemia or lymphoma cell.
Major identifying cell surface markers for immune cells include CD34 and c-kit for Hematopoietic stem cells (HSC).
Antigens are defined as an organism, molecule, or part of a molecule that is recognized by the immune system.
The immune system can recognize altered self, which refers to changes in the body's cells after infection or malignant transformation.
Altered self antigens may be mutated gene products or normal proteins expressed at higher levels due to aberrant regulation.
Microorganisms bear repeating patterns of molecular structure on their surface, known as PAMPs or DAMPs.
PAMPs are specific targets of the immune system and include structures like the cell walls of Gram-positive and Gram-negative bacteria.
Innate immune cells use receptors that are germline encoded to recognize pathogen-associated antigens.
Each B or T cell expresses only one type of receptor, which is always on the cell surface, although B cells can secrete their receptors in the form of antibodies.
Table listing major identifying cell surface markers includes Hematopoietic stem cell, B cell, T cell, and NK cell with their corresponding CD markers. 
The receptors used in innate immunity are located in the plasma membrane, endosomal membrane, and cytosol.
Innate immunity has about 100 different types of invariant receptors, while adaptive immunity has only 2 types of receptors (Ig and TCR).
The number of unique antigens recognized by the adaptive immune system is estimated to be greater than 10^7.
The contraction phase of the immune response results in about 10^4 T cells remaining after the response.
The early innate defense relies on invariant, germline-encoded receptors recognizing common features of pathogens.
Adaptive immunity provides enhanced protection against reinfection by recognizing a particular pathogen.
The classic cadence of the immune response shows the number of microbe-specific T cells over time, indicating phases of clonal expansion and contraction.
The graph depicting the classic cadence of the immune response shows the number of CD8+ T cells and CD4+ T cells over days after infection.
The innate immune system is crucially important but has limitations as it can be overcome by many pathogens.
Adaptive immunity is characterized by the formation of memory cells after an initial response to a pathogen.
The discrimination of self and nonself in innate immunity is based on the recognition of healthy host cells that do not express certain molecules.
In adaptive immunity, self-reactive lymphocytes are eliminated or inactivated to avoid autoimmunity.
In adaptive immunity, receptors are formed by somatic recombination of gene segments only in B and T cells.
The table comparing innate and adaptive immunity features highlights differences in specificity, microbial molecules recognized, receptors, distribution, genes, and self-non-self discrimination. See the comparison table for details: 
The innate immune response fails to eliminate a new infection, leading to activated antigen presenting cells being delivered to the draining lymph nodes.
When a recirculating lymphocyte encounters its corresponding antigen, it is induced to proliferate and differentiate into effector B or T lymphocytes.
A subset of proliferating lymphocytes differentiates into memory cells, which are ready to respond rapidly to the same pathogen if encountered again.
After infection clears, antigen-specific lymphocytes gradually decrease from its peak in a phase called resolution phase.
Following resolution, antigen-specific lymphocytes are sustained at a level that is slightly higher than prior to infection, contributing to immunological memory.
The immune system defends the body against infection, with the innate immune system acting quickly but lacking the ability to recognize certain pathogens.
Adaptive immunity is based on clonal selection from a repertoire of lymphocytes bearing highly diverse antigen-specific receptors.
Host defense requires different recognition systems and a wide variety of effector mechanisms to seek out and destroy diverse pathogens.
The innate immune system provides non-specific protective immunity, while adaptive immunity provides specific protective immunity that prevents reinfection.
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