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Development of the immune system

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Why is the immune response in early life dampened compared to adults?

Back (Answer)

• Due to immunosuppresive environment of the womb • Adapted to the new antigens in early life - response skewed to suppression

#2
Front (Question)

The reduction in immune responses leads to increased susceptibility to pathogens + to reduced responses to vaccines. What evidence shows this?

Back (Answer)

• Peak age of serious bacterial infections is <5yo • Highest rate of meningitis of any age group is in newborns

#3
Front (Question)

The altered function of the neonatal immune response may also influence the development of what conditions in later life?

Back (Answer)

Asthma and allergy

#4
Front (Question)

Key components of the immune system are the non-antigen specific and the antigen-specific systems. Describe key features of the non-antigen specific immune system

Back (Answer)

• Less sophisticated, more primitive components • Barriers: skin + mucosa • Cells: neutrophils, monocytes, macrophages • Soluble components: complement, cytokines

#5
Front (Question)

Describe the antigen-specific part of the immune system

Back (Answer)

• More sophisticated • Respond to specific antigens • Commited to immune memory • Rapid enhanced responses on subsequent exposure to antigen • T + B lymphocytes

#6
Front (Question)

What are the primary lymphoid organs?

Back (Answer)

• Thymus • Bone marrow

#7
Front (Question)

What are the secondary lymphoid organs?

Back (Answer)

• Spleen • Lymph nodes • Tonsils • Peyer’s Patches • Bronchus

#8
Front (Question)

What is the thymus?

Back (Answer)

• Glandular organ near the heart • T cells learn their job here

#9
Front (Question)

What is bone marrow?

Back (Answer)

• Blood-producing tissue located inside certain bones • Blood stem cells give rise to all of the diff types of blood cells

#10
Front (Question)

What is the role of the spleen?

Back (Answer)

• Serves as a filter for the blood • removes old + damaged RBCs • removes infectious agents + uses them to activate cells called lymphocytes

#11
Front (Question)

What are lymph nodes?

Back (Answer)

Small organs that filter out dead cells, antigens + other “stuff” to present to lymphocytes

#12
Front (Question)

What do lymphatic vessels do?

Back (Answer)

Collect fluid (lymph) that has “leaked” out from the blood into the tissues + returns into circulation

#13
Front (Question)

What are the 4 stages of development of immunity in a human fetus?

Back (Answer)

• Mesoblastic: 18 days -> 10 weeks • Hepatic: 6-8 weeks -> birth • Splenic • Myeloid: 10-12wks -> 20wks gestation

#14
Front (Question)

Which immunity development stage is responsbile for the major site of blood cell formation?

Back (Answer)

• Myeloid

#15
Front (Question)

In regards to development of immune responsiveness in human fetus, what developments occur from 4 to 11 weeks of gestation?

Back (Answer)

• 4 - macrophages in yolk sac • 5 - complement synthesis detectable • 6 - Natural Killer cells present in liver • 6-7 - thymic epithelium develops • 7 - lymphocytes + macrophages in blood • 7-9 - lymphocytes in thymus • 11 - serum IgM detectable in infection + mitogen responsiveness of thymocytes

#16
Front (Question)

In regards to development of immune responsiveness in human fetus, what developments occur from 12 to 20 weeks of gestation?

Back (Answer)

• 12-14 - neutrophils in blood • 13 - B cells in bone marrow • 14 - mitogen responsiveness of peripheral lymphocytes • 17 - IgG in serum - infection only • 20 - alloreactivity detectable

#17
Front (Question)

Describe how the T cells develop

Back (Answer)

• T cells migrate from bone marrow -> THYMUS • Gene rearrangements + maturation occur • Each T cell undergoes gene rearrangements to prod a unique antigen receptor on cell surface • Mature T cells leave thymus + re-circulate through secondary lymphoid tissues

#18
Front (Question)

What is the thymus derived from?

Back (Answer)

3rd pharyngeal pouch

#19
Front (Question)

What is the thymus composed of and how does it develop?

Back (Answer)

• Thymic epithelium + medulla • @ GA 8w - colonization of the thymus by HSC (haemopoetic stem cells) • @ GA 20w - thymus is developed • @ GA 16-20w - T cells emigrate to periphery

#20
Front (Question)

The other part of the antigen-specific immune system is B cells - describe the development of B cells

Back (Answer)

• Bone marrow produces B cells from primitive stem cells • Migration to secondary lymphoid organs eg. spleen, lymph nodes • Each B cell expresses immunoglobulin on its surface - of single antigenic specificty • Ongoing gene rearrangements results in immature B cells with diverse repertoire of surface Ig molecules ready for selective events driven by antigen binding -> develop memory B cells for faster, more specific response

#21
Front (Question)

Why will a baby be born with a lot of IgG antibody and how does this level change throughout life?

Back (Answer)

Newborns are deficient in their own-generated specific antibodies. This is partly alleviated by trans-placental active transfer of maternal IgG antibody. These IgG antibodies will be broken down and metabolised by around 3 months of age, so will be at its lowest then but IgG begins to increase slowly after that. Reaches adult levels around 5 years of age.

#22
Front (Question)

There are different classes of IgG - which ones are transferred first across the placenta?

Back (Answer)

IgG1 and IgG3 before IgG2+4

#23
Front (Question)

In terms of development of the non-antigen specific immune system, when are granulocytes present from and what are they like comp to adults?

Back (Answer)

• From 31w GA • High number but less effective: motility + transendothelial migration reduced • Adherence + phagocytosis similar to adult

#24
Front (Question)

Describe the development of complement proteins

Back (Answer)

• Series of serum proteins that function as enzymatic cascade • Until 6-18 months of age conc of most C’ lower than in adults • Reduced function in children