Is the most abundant class of antibodies in plasma during secondary immune response?

Primary Immune Response

Memory B-cells are long-lived plasma cells that are formed mainly in the germinal centres.

Firstly, during the primary immune response, naïve B-cells are activated by T-cells. after that, B-cells move to secondary lymphoid organs like the spleen and lymph nodes where they enter B-cell follicles or germinal centres within the cortex.

Inside the germinal centre, B-cells proliferate and undergo somatic hypermutation which changes the affinity of their receptor. The receptors are then tested for their affinity within the germinal centre.

In summary, B-cells that can bind their antigens on follicular dendritic cells subsequently receive survival signals from T-cells, while those that do not bind or bind with less affinity are outcompeted and undergo apoptosis. Moreover, B-cells will class switch from IgM to other antibody types such as IgA or IgG.

After somatic hypermutation and class-switching, B-cells differentiate into plasma cells and memory B-cells. Plasma cells are short-lived and die quickly following the primary immune response.

On the other hand, memory cells are long-lived and relocate to the periphery where they are more likely to encounter antigen on re-exposure. Many of the circulating B-cells become concentrated in areas of the body where there is a high likelihood of encountering antigen, such as in Peyer’s patches.

Sciencia58 an the makers of the single images Domdomegg, [1], Fæ, Petr94, Manu5, CC BY-SA 4.0

, via Wikimedia Commons

Is the most abundant class of antibodies in plasma during secondary immune response?

Fig 1 – Diagram summarising some of the processes involved in the primary immune response

Secondary Immune Response

When these memory cells meet their specific antigen again, they rapidly proliferate and differentiate into plasma cells. These plasma cells then respond by producing abundant quantities of antibody to clear the antigen.

A subset of these memory cells can also go into the germinal centres for further class switching and affinity maturation. Memory B-cells can also activate effector T-cells by presenting antigen on MHC-II molecules.

The process of differentiation from memory B-cell to plasma cell is quicker than if they have differentiated from naïve B cells. Memory cells can survive for decades and so can respond to multiple exposures over time. Furthermore, they do not require continual interaction with antigen or T-cells to survive. As they have already undergone class switching and affinity maturation, they can divide faster and produce higher affinity antibodies such as IgG in response to antigen.

Memory T Cells

For memory T-cells, see this page.

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, via Wikimedia Commons

Is the most abundant class of antibodies in plasma during secondary immune response?

Fig 2 – Graph showing the difference in antibody production between the primary and secondary immune response

Overview of Immune Responses

The table below summarises some key differences between the primary and secondary immune responses:

  Primary immune response Secondary immune response
Responding cells

Naïve B and T cells

Memory B and T cells

The threshold for activation (i.e., the dose of antigen needed to initiate response)

High

Low

Onset of response

Slow

Quick

Rate of antibody production

Low

High

Lag phase (time between antigen exposure and antibody detection)

Long lag phase (4-7 days)

Short lag phase (1-3 days)

Time to peak antibody response

 7-10 days

 3-5 days

Antibody types

IgM >>>IgG

IgG >>> IgM

IgA and IgE may also be present

Antibody affinity

Low-affinity antibodies

High-affinity antibodies

Response magnitude

Depends on the antigen, but antibody levels are relatively low and decline rapidly

100-1000x higher than the primary response; antibody titres remain high for longer periods of time

Immunity

Slow control of infection

Rapid control of infection

T cell activation

Delay before effector T cells are activated

Effector T cells are present and can act immediately.

Innate immune system

Innate immunity works alone until the adaptive response is initiated

The adaptive and innate immune system work together from the start

Clinical Relevance – Vaccinations

The principle of T-cell memory is exploited through vaccinations. A vaccine contains weakened or dead forms of the pathogen and is designed to mimic the initial exposure.

Upon entry, the dead or weakened pathogen is captured and presented on APCs which stimulates the innate immune response. Consequently, this leads to the differentiation of naïve T cells and the expansion of T and B cell populations.

Although there is no clinical infection to fight in this scenario, the vaccine enables the production of T-memory cells so that should a live form of this pathogen enter the body the immune system is already prepared to fight it.

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Is the most abundant class of antibodies in plasma during secondary immune response?

Fig 3 – Graph showing the immune response in the body following vaccination and reinfection – the response is much faster on reinfection due to B and T cell memory cells in the immune system

Which antibody is most abundant during secondary immune response?

The major class of immunoglobulin in the blood is IgG, which is a four-chain monomer produced in large quantities during secondary immune responses.

What antibody class is most abundant in plasma?

IgG is the most abundant antibody isotype in the blood (plasma), accounting for 70-75% of human immunoglobulins (antibodies). IgG detoxifies harmful substances and is important in the recognition of antigen-antibody complexes by leukocytes and macrophages.

Which antibody class is produced during the secondary immune response?

IgG is the antibody produced by most memory cells, but IgA- and IgE-expressing B cells play an important role in secondary immune response, too.

Is IgG a secondary response?

IgG is synthesized mostly in the secondary immune response to pathogens. IgG can activate the classical pathway of the complement system, and it also is highly protective. The four subclasses of IgG include IgG1, IgG2, IgG3, and IgG4.