Chapter 29 Types of Vaccines Flashcards

1
Q

What is active immunization in equine medicine?

A

The use of antigens formulated as a vaccine to stimulate an immune response.

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2
Q

What is re-immunization in horses?

A

Natural exposure to the pathogen in the vaccinated animal, resulting in a secondary immune response and enhanced immunity.

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3
Q

What is the ideal characteristic of a vaccine?

A

It should be safe, induce a potent and long-lasting immune response, not cause clinical signs of the disease, and have minimal or no adverse side effects.

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4
Q

What are the types of vaccines licensed for use in horses?

A

Attenuated or modified live vaccines (MLV), killed or inactivated vaccines, subunit vaccines, nucleic acid-based vaccines, and chimera vaccines.

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5
Q

What is an attenuated or modified live vaccine (MLV)?

A

A vaccine composed of viable attenuated organisms that replicate in host cells and stimulate an immune response without causing disease.

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6
Q

What are the principal advantages of MLVs?

A

They are usually more effective than killed or inactivated vaccines, stimulate both innate and adaptive immune responses, and elicit a greater number of effector mechanisms.

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7
Q

What are the disadvantages of MLVs?

A

Potential for virulence reversion, opportunistic infections in immunodeficient patients, challenging manufacturing, storage, handling, safety, and phenotypic stability issues.

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8
Q

What is an example of an intranasal MLV for equine influenza virus?

A

Flu Avert, attenuated by cold adaptation in embryonated eggs.

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9
Q

What is a killed or inactivated vaccine?

A

A vaccine prepared with microorganisms that are rendered unable to replicate in the host through chemical, heat, or irradiation methods.

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10
Q

What are the advantages of killed or inactivated vaccines?

A

Easier to manufacture, more stable than live vaccines, cannot revert to virulent form, and safer for immunosuppressed animals.

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11
Q

What is the main disadvantage of killed or inactivated vaccines?

A

They usually require multiple injections to elicit an immune response and generally induce less adverse reactions.

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12
Q

What is an example of a killed vaccine against West Nile virus?

A

West Nile Innovator, shown to provide protection against severe disease.

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13
Q

What is a protein or subunit vaccine?

A

A vaccine that combines a portion of the pathogen, such as purified antigens or inactivated toxins, usually combined with an adjuvant.

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14
Q

What are the advantages of subunit vaccines?

A

Increased safety without risk of reverting to virulence, reduced antigenic competition, and potential to differentiate vaccinated from infected animals.

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15
Q

What are the disadvantages of subunit vaccines?

A

Require strong adjuvants, may cause tissue adverse reactions, generally shorter duration of immunity, do not generate mucosal antibodies, and do not replicate intracellularly.

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16
Q

What is an example of a subunit vaccine for Streptococcus equi?

A

Strepvax II, made with a purified M-protein.

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17
Q

What is a recombinant vectored vaccine?

A

A vaccine that uses a virus or bacterium vector to express selected genes from the target pathogen coding for protective antigens.

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18
Q

What is the advantage of viral vector vaccines?

A

Induction of a full range of immune responses, including cytotoxic T lymphocytes (CTLs).

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19
Q

What is the main concern with vectored vaccines?

A

Pre-existing immunity against the vector or potential immune response against the vector limiting response to the target pathogen.

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20
Q

What is an example of a canary pox-vectored vaccine for equine influenza virus?

A

Recombitek rFLU, expressing genes for the hemagglutinin of two influenza virus lineages.

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21
Q

What is a DNA-based vaccine?

A

A vaccine produced by inserting genes coding for protective antigens into bacterial plasmids that enter host cells and direct the synthesis of the vaccine protein.

22
Q

What are the advantages of DNA vaccines?

A

Safe, stable, easy and inexpensive to manufacture, elicit strong CTL responses, and have intrinsic adjuvant-like activities.

23
Q

What are the disadvantages of DNA vaccines?

A

Decreased DNA uptake with increased body size, potential for chronic inflammation or autoantibody production, limited to protein immunogens, and potential to affect genes responsible for cell growth.

24
Q

What was the first USDA-approved DNA vaccine for horses?

A

West Nile-Innovator DNA, for West Nile virus.

25
Q

What is a chimera vaccine?

A

A hybrid organism created by combining nucleic acid fragments from two or more different organisms, with at least two fragments containing essential genes necessary for replication.

26
Q

What is an example of a chimera vaccine for West Nile virus?

A

PreveNile, a live West Nile virus flavivirus chimera.

27
Q

What is a marker vaccine (DIVA)?

A

A vaccine that lacks one or more proteins of the virulent organism, enabling differentiation of vaccinated animals from those infected naturally.

28
Q

What is an example of a marker vaccine for equine arteritis virus?

A

A recombinant EAV with a silent nucleotide substitution in the nucleocapsid gene.

29
Q

What type of immune responses do vaccines induce?

A

Development of antibodies, long-lived effector cells, and memory cells.

30
Q

What influences the type of immune response elicited by a vaccine?

A

The type of vaccine, antigen load, adjuvant or delivery system, and host factors such as genetics, existing immunity, age, immune status, presence of maternal antibodies, and pregnancy status.

31
Q

What is the role of innate immunity in vaccination?

A

Sending danger signals to the host through stimulation of pathogen recognition receptors (PRRs) of the innate immune cells.

32
Q

What are examples of pathogen recognition receptors (PRRs)?

A

Toll-like receptors (TLRs) and NOD-like receptors (NLRs).

33
Q

How do live vaccines stimulate the innate immune system?

A

By containing pathogen-associated molecular patterns (PAMPs) regardless of attenuation.

34
Q

What is the role of adjuvants in inactivated, subunit, or DNA vaccines?

A

To promote inflammation at the site of vaccination and attract antigen-presenting cells (APCs) that initiate T and B cell activation.

35
Q

What is humoral immunity?

A

An immune response involving the production of antibodies that control extracellular infections.

36
Q

What happens to antigens after injection of a vaccine?

A

They reach the regional lymph nodes or spleen, where they are stored on the surface of follicular cells of lymphoid tissues.

37
Q

What are the two signals required for B cell activation?

A

Binding of antigens to the B cell receptor (BCR) and subsequent interaction with CD4+ T helper cells.

38
Q

What are T cell-independent antigens?

A

Antigens that induce strong B cell activation without the need of T cell interaction.

39
Q

What is cell-mediated immunity (CMI)?

A

An immune response involving the activation of T cells to control intracellular pathogens.

40
Q

What is the advantage of modified-live vaccines in inducing CMI responses?

A

They are effective at inducing CMI responses by activating CD4+ T helper cells and cytotoxic CD8+ T cells.

41
Q

What is the role of antigen-presenting cells (APCs) in vaccination?

A

To migrate to lymphoid tissues from the site of injection, process the vaccine antigen, and present it to CD4+ T cells via MHC class II molecules.

42
Q

What happens to T cells after activation by APCs?

A

They undergo clonal expansion and differentiation into effector cells.

43
Q

What is the role of CD4+ T helper effector cells?

A

To produce cytokines that activate B cells, CD8+ T cells, and macrophages.

44
Q

What is the role of CD8+ T cells (CTLs)?

A

To mediate cytotoxicity of host cells containing intracellular pathogens.

45
Q

What are the different routes of vaccination?

A

Intramuscular, subcutaneous, intranasal, oral, sublingual, vaginal, ocular, and aerosol.

46
Q

Why is the route of administration important in vaccine development?

A

To reach local APCs and induce immunity similar to a natural challenge.

47
Q

What are mucosal vaccines?

A

Vaccines designed to generate mucosal immunity by mimicking natural infection at the site of pathogen entry.

48
Q

What are examples of mucosal pathogens?

A

Equine influenza virus (EIV), equine herpesvirus-1 (EHV-1), Streptococcus equi, Rhodococcus equi, Salmonella enterica, and Escherichia coli.

49
Q

What are the advantages of needle-free vaccine delivery?

A

Efficiency and effectiveness comparable to parenteral administration with a syringe and needle.

50
Q

What are adjuvants?

A

Substances added to vaccines to enhance and modulate protective immunity.

51
Q

What are the proposed mechanisms of action of adjuvants?

A

Formation of depot, induction of inflammatory cytokines and chemokines, recruitment of immune cells, enhancement of antigen uptake and presentation, and increased expression of costimulatory molecules and cytokines.