Chapter 11_2 flashcards

(60 cards)

1
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2
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Immune System: Primary Function

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A complex defense mechanism that protects humans from injurious environmental agents by deciphering “self” versus “non-self” substances. Non-self substances (foreign antigens) are targeted for destruction.

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3
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Innate Immunity: Definition & Key Components

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The body’s first and immediate, non-specific line of defense. Components include: natural anatomical barriers (skin, mucous membranes), normal flora, white blood cells (WBCs like macrophages), and protective enzymes/chemicals (interferon, cytokines, hydrochloric acid).

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4
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Adaptive Immunity: Definition & Key Characteristics

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The immune system’s second line of defense, developed after exposure to antigens. Characteristics: specificity (targets specific antigens), memory (remembers antigens for future encounters), rapid and destructive response upon re-exposure. Involves B and T lymphocytes.

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5
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Differentiate: Innate vs. Adaptive Immunity

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Innate: Immediate, non-specific, no memory, first line of defense (barriers, phagocytes, NK cells). Adaptive: Delayed (develops after exposure), specific, has memory, second line of defense (B cells/antibodies, T cells).

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6
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Antibody-Mediated (Humoral) Immunity: Mechanism

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A type of adaptive immunity where B lymphocytes, upon encountering an antigen and with T-cell help, differentiate into plasma cells. Plasma cells produce and secrete specific proteins called immunoglobulins (antibodies) that neutralize or eliminate extracellular antigens.

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7
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Cell-Mediated Immunity: Mechanism

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A type of adaptive immunity mediated by T lymphocytes. CD8+ cytotoxic T cells directly kill infected host cells or tumor cells. CD4+ helper T cells coordinate the immune response by releasing cytokines that activate other immune cells (including B cells, macrophages, and other T cells).

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8
Q

Compare: Antibody-Mediated vs. Cell-Mediated Immunity

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Both are adaptive. Antibody-mediated (Humoral): B cells -> plasma cells -> antibodies; targets extracellular pathogens/toxins. Cell-mediated: T cells (CD4+ helper, CD8+ cytotoxic); CD8+ directly kill infected cells, CD4+ help activate/regulate immune responses.

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9
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Types of Immune Dysfunction: Overview

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  1. Immunodeficiency: Weakened immune system unable to destroy foreign invaders. 2. Autoimmunity: Immune system fails to distinguish self from non-self, attacking body’s own tissues. 3. Hypersensitivity: Overreactive immune response against foreign invaders or self-antigens, causing tissue damage (e.g., allergies, transplant rejection).
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10
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Antigen: Definition

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Any substance, usually foreign, that is recognized by the immune system as non-self and is capable of eliciting an immune response, such as the production of antibodies or the activation of T lymphocytes.

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11
Q

Major Histocompatibility Complexes (MHCs) / Human Leukocyte Antigens (HLAs)

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Surface proteins found on nearly all human cells that present antigen fragments to T cells. They allow the adaptive immune system to distinguish between “self” (host cells) and “non-self” (foreign or infected cells). Crucial for antigen presentation and immune recognition.

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12
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Monocyte-Macrophages: Origin & Functions

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Macrophages arise from monocytes (a type of WBC) that migrate from peripheral circulation into tissues. Functions: Phagocytosis of debris/antigens, antigen presentation to T cells, mediation of innate immunity, cytokine production, breakdown of antigens with secretory products (hydrolytic enzymes, TNF-alpha, ILs).

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13
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Cytokines: Definition & General Roles

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Inflammatory mediators produced mainly by WBCs (macrophages, lymphocytes). Roles: Promote leukocyte recruitment, regulate lymphocyte growth/activation/differentiation, activate macrophages, stimulate hematopoiesis (new blood cell production). Examples: TNF-alpha, interleukins (ILs).

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14
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Natural Killer (NK) Cells: Role in Immunity

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A type of lymphocyte that is part of the innate immune response. NK cells act as a first line of defense by directly destroying tumor cells and virus-infected cells without prior sensitization or antigen presentation via MHC.

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15
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Lymphocytes: Origin & Maturation

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Primary cells of adaptive immunity. Originate from stem cells in the bone marrow in immature form.
T lymphocytes (T cells): Mature in the thymus gland.
B lymphocytes (B cells): Mature in the bone marrow, spleen, and lymph nodes.

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16
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T Lymphocytes (T cells): General Role & Maturation Site

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Key players in cell-mediated adaptive immunity. Mature in the thymus gland. Differentiate into various subtypes, including CD4+ helper T cells and CD8+ cytotoxic T cells.

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17
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B Lymphocytes (B cells): General Role & Maturation Sites

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Key players in antibody-mediated (humoral) adaptive immunity. Mature in bone marrow, spleen, and lymph nodes. When activated by antigen (with T-cell help), they differentiate into plasma cells (antibody-producing) and memory B cells.

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18
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CD4+ Cells (T Helper Cells): Functions

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A type of T lymphocyte that plays a central role in orchestrating the immune response. They recognize antigens presented by APCs on MHC class II molecules. Functions: Help activate B cells to produce antibodies, enhance activity of cytotoxic T cells, activate macrophages, and release cytokines that regulate other immune cells. Main target of HIV.

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19
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CD8+ Cells (Cytotoxic T Cells): Functions

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A type of T lymphocyte that directly kills host cells infected with viruses or other intracellular pathogens, as well as tumor cells. They recognize antigens presented on MHC class I molecules on the surface of target cells.

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20
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Antigen-Presenting Cells (APCs): Role & Examples

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Cells that capture, process, and present antigens to T lymphocytes to initiate an adaptive immune response. Examples: Dendritic cells (most potent, broadest range of antigen attachment), macrophages, and B cells.

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21
Q

Dendritic Cells: Description & Function

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Potent APCs named for their fine dendritic cytoplasmic projections. Located in epidermis and mucous membranes (where antigens enter). They capture and process antigens, then migrate to lymph nodes to present them to T cells, initiating innate and adaptive responses by releasing cytokines.

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22
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Plasma Cells: Origin & Function

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Differentiated B lymphocytes that are specialized in producing and secreting large quantities of specific antibodies (immunoglobulins). They are the effector cells of humoral immunity.

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23
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Immunoglobulins (Igs) / Antibodies: Definition & General Functions

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Proteins produced by plasma cells in response to a specific antigen. Functions: Neutralize bacterial toxins, attack viruses, promote phagocytosis of bacteria, activate the complement system, and play a role in allergic reactions and immune regulation. Five main classes: IgM, IgG, IgA, IgE, IgD.

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24
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Immunoglobulin M (IgM): Characteristics & Significance

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Largest immunoglobulin (macroglobulin). The first antibody class produced during a primary immune response (earliest responder to infection). Effective in activating complement. Due to its large size, it generally does not cross the placenta.

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25
Immunoglobulin G (IgG): Characteristics & Significance
Most abundant immunoglobulin in the bloodstream and tissue fluids. The predominant antibody in the secondary immune response (amnestic response). Crosses the placenta, providing passive immunity to the fetus/newborn. Involved in opsonization, complement activation, and neutralization of toxins/viruses. Commonly involved in autoimmune diseases.
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Immunoglobulin A (IgA): Characteristics & Significance
The main immunoglobulin found in mucosal secretions (tears, saliva, nasal/respiratory secretions, GI fluid, breast milk). Provides localized protection on mucosal surfaces against pathogens. Also called secretory IgA.
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Immunoglobulin E (IgE): Characteristics & Significance
Present in very low concentrations in blood but rises significantly in allergic reactions and parasitic infections. Binds to high-affinity receptors on mast cells and basophils, triggering release of histamine and other mediators upon antigen binding. Abundant in skin, mucous membranes, respiratory tract.
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Immunoglobulin D (IgD): Characteristics & Significance
Found in small amounts in serum, primarily located on the surface of naive B lymphocytes, where it functions as an antigen receptor involved in B cell activation. Also binds to basophils and mast cells in hypersensitivity reactions.
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Primary Immune Response: Description
The immune response that occurs upon the first exposure to a specific antigen. Characterized by a lag phase (5-7 days for IgM to be detected) while B cells are activated and differentiate into plasma cells. IgM is the predominant antibody produced initially.
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Secondary (Amnestic) Immune Response: Description
The immune response that occurs upon subsequent exposures to the same antigen. It is faster, stronger, and more prolonged than the primary response due to the presence of memory B and T cells. IgG is the predominant antibody produced.
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Active Acquired Adaptive Immunity: Definition & Examples
Immunity developed by an individual's own immune system after exposure to an antigen. This can occur through natural infection (contracting the disease) or through vaccination. Results in long-lasting protection due to the formation of memory cells.
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Passive Acquired Adaptive Immunity: Definition & Examples
Immunity acquired by receiving pre-formed antibodies from another source, rather than producing them oneself. Examples: Maternal IgG crossing the placenta to the fetus, IgA in breast milk, or administration of immune globulin (e.g., HBIg for hepatitis B exposure). Provides immediate but temporary protection (no memory cells formed).
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Vaccine: Definition & Purpose
A biological preparation containing a weakened (attenuated), killed (inactivated) pathogen, its toxins (toxoid), or one of its surface proteins (subunit/mRNA). Administered to stimulate the recipient's adaptive immune system to develop active acquired immunity and memory against a specific disease without causing the disease itself.
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Types of Vaccines Mentioned in Text
1. Live virus vaccines (inactivated/attenuated): Stimulate immune response but typically non-disease producing (e.g., oral poliovirus - though potential for mutation). 2. mRNA vaccines: Synthesized from viral pathogen's mRNA coding for a surface protein; patient's body manufactures the protein, triggering an immune response. 3. Bacterial vaccines: Derivatives of killed microorganisms or extracts of antigens or toxins. 4. Toxoids: Modified bacterial toxins that are non-disease producing but still antigenic (e.g., tetanus toxoid).
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Booster Vaccination: Purpose
An additional dose of a vaccine administered after the primary vaccination series to "boost" or restimulate the immune system's memory response, thereby increasing the level and duration of immunity against the specific antigen.
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Toxoid: Definition & Example
A type of vaccine made from a bacterial toxin that has been modified to be non-toxic but still capable of stimulating an immune response (i.e., it retains its antigenicity). Example: Tetanus toxoid vaccine.
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Vaccination / Immunization: Definition
Vaccination: The act of administering a vaccine. Immunization: The process by which an individual becomes protected against a disease through vaccination or prior infection, resulting in the development of active acquired immunity.
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Anergy Panel: Purpose & Interpretation
A test of general immunocompetence. It involves intradermal injection of common antigens (e.g., mumps, Candida) to which most individuals have been exposed. Positive reaction (redness, induration): Indicates immunocompetence. No reaction (anergy): Suggests a lack of immune responsiveness or immunodeficiency.
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Antibody Titer / Antibody Screening: Purpose & Interpretation
Laboratory tests used to measure the presence and level (titer) of specific antibodies (IgM and IgG) in the blood. Purpose: Confirm adequate immune protection against a particular antigen, diagnose current/past infection. Interpretation: Elevated IgM often indicates recent/current infection. Elevated IgG indicates past exposure and immunity.
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Allergy Testing: Methods Mentioned
1. Skin Tests: Measure IgE reaction to allergens by scratching/injecting small amounts into skin. Positive = redness, swelling, itching. 2. Serology Blood Tests (ELISA, RAST, ImmunoCAP IgE): Measure presence and amount of allergen-specific IgE in blood to evaluate severity of allergy.
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Hypersensitivity: General Definition
An exaggerated or inappropriate immune response to an antigen (allergen or autoantigen) that results in tissue damage and disease. Can involve cell-mediated or antibody-mediated mechanisms. Four main types (I, II, III, IV).
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Type I Immediate Hypersensitivity: Basic Mechanism
Rapidly developing immune reaction after IgE binds to mast cells and combines with antigen. Involves CD4 cells, IgE, eosinophils, and mast cells. Mast cell degranulation releases histamine and other mediators, causing allergy symptoms.
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Type II Cytotoxic Hypersensitivity: Basic Mechanism
Mediated by Igs (IgG or IgM) directed towards antigens present on cell surfaces. Antibodies target cells coated with antigen, leading to cell destruction via complement activation or phagocytosis.
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Type III Immune Complex Hypersensitivity: Basic Mechanism
Occurs when antigen combines with Ig (antibody) within circulation, forming immune complexes. These complexes deposit in tissues, triggering inflammation and organ dysfunction.
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Type IV Delayed Hypersensitivity: Basic Mechanism
Initiated by T lymphocytes (sensitized T cells) that have had previous exposure to an antigen. Reaction (inflammation, e.g., contact dermatitis) occurs days after re-exposure due to T cell cytokine release.
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Autoimmunity: General Definition
A state where the immune system fails to distinguish between self and non-self antigens, leading to an immune response against the body's own tissues and cells. Involves autoantibodies or autoreactive T cells.
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Immunodeficiency: General Definition
A state in which the immune system's ability to fight infectious disease and cancer is compromised or entirely absent. Can be primary (congenital) or secondary (acquired).
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Atopic Disorder: Definition
A term often used to describe a group of allergic conditions that are often inherited and include eczema (atopic dermatitis), allergic rhinitis (hay fever), and asthma. Associated with a tendency to produce IgE antibodies in response to common environmental allergens.
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HIV: Nature of Virus (Retrovirus, Lentivirus)
HIV (Human Immunodeficiency Virus) is a retrovirus, meaning its genetic material is RNA, and it uses the enzyme reverse transcriptase to convert its RNA into DNA within the host cell. It belongs to the *Lentivirus* genus, characterized by a long incubation period and slowly progressive disease course.
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Reverse Transcriptase (HIV Enzyme): Role
An enzyme unique to retroviruses like HIV. It converts the viral RNA genome into a double-stranded DNA copy, which can then be integrated into the host cell's DNA. A major target for antiretroviral drugs (NRTIs, NNRTIs).
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Integrase (HIV Enzyme): Role
An HIV enzyme that facilitates the insertion (integration) of the viral DNA (produced by reverse transcriptase) into the host cell's chromosomal DNA. This makes the infection permanent for that cell. A target for antiretroviral drugs (INSTIs).
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Protease (HIV Enzyme): Role
An HIV enzyme essential for the late stages of viral replication. It cleaves newly synthesized large viral polyproteins into smaller, functional proteins that are necessary for assembling mature, infectious virus particles. A target for antiretroviral drugs (PIs).
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CCR5 Receptor & CXCR4 Receptor: Role in HIV Infection
Chemokine co-receptors found on the surface of target cells (like CD4+ T cells and macrophages). HIV uses one or both of these (in addition to the CD4 receptor) to bind to and enter host cells. CCR5 antagonists are a class of ART.
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HIV Resistors (CCR5 Gene Mutation)
Individuals who have a specific genetic mutation (deletion) in the CCR5 gene (homozygous for CCR5-delta32 mutation) lack functional CCR5 co-receptors on their cells. This makes them highly resistant to infection by HIV strains that use CCR5 for entry (R5-tropic viruses).
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Viral Load (HIV RNA Assay): Concept & Significance
Measures the amount of HIV genetic material (RNA copies) in a milliliter of blood. It is the most accurate measure of viral replication. Significance: Indicates disease severity, risk of progression to AIDS, and effectiveness of antiretroviral therapy. Goal of ART is an undetectable viral load.
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Seroconversion (HIV): Concept
The point in time when an individual infected with HIV develops detectable levels of antibodies against the virus in their bloodstream. Typically occurs 2 weeks to 6 months after infection. Before seroconversion, antibody tests may be negative despite active infection (window period).
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Window Period (HIV): Concept
The time between initial HIV infection and the development of detectable antibodies. During this period (typically 2 weeks to 6 months), an infected person can transmit the virus but may test negative on standard HIV antibody tests. HIV RNA or p24 antigen tests can detect infection earlier.
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p24 Antigen Test (HIV): Concept
A test that detects the p24 protein, a core structural protein of the HIV capsid. p24 antigen levels are high in the bloodstream shortly after infection (around day 14), before antibodies are detectable, and can decline after seroconversion. Often used in combination antibody/antigen screening tests for earlier diagnosis.
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Opportunistic Infection: General Definition
An infection caused by a pathogen (bacterium, virus, fungus, or parasite) that usually does not cause disease in a healthy individual but can cause disease in an individual with a weakened immune system (immunocompromised host), such as someone with AIDS or undergoing immunosuppressive therapy.
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Antiretroviral Therapy (ART): General Definition
A treatment regimen for HIV infection consisting of a combination of different antiretroviral drugs that suppress HIV replication by targeting various stages of the viral life cycle. ART does not cure HIV but can control the virus, preserve immune function, and prevent progression to AIDS.