Immune responses to antigens may be categorised as primary or secondary responses. The primary immune response of the body to antigen occurs on the first occasion it is encountered. Depending on the nature of the antigen and the site of entry this response can take up to 14 days to resolve and leads to the generation of memory cells with a high specificity for the inducing antigen. The humoral response, mediated by B cells with the help of T cells, produces high-affinity and antigen-specific antibodies. This is in contrast with the CD8 T-cell response which leads to the generation of large numbers of antigen-specific cells that are capable of directly killing infected cells. Antigen-specific CD4 T cells, which provide help to B cells in the form of cytokines and other stimulatory factors, can also be expanded upon antigenic stimulation.
The secondary response of both B- and T cells is observed following subsequent encounter with the same antigen and is more rapid leading to the activation of previously generated memory cells. This has some quantitative and qualitative differences from the primary response.
Key Concepts:
The innate immune system is the first line of defence against infectious agents. When this is breached, the adaptive immune system provides a more efficient response to clearing pathogens.
The adaptive immune system has the capacity to ‘remember’ previous antigens, a process termed immunological memory.
Antigen-specific T cells are selected during a primary immune response and expand to produce clones of T cells with high specificity for the activating antigen.
In a B cell primary response to a thymus-dependent antigen, the immune system selects B cells with a high affinity and specificity for the antigen and these become memory cells.
The selection of B cells with a high affinity for a given antigen occurs in the germinal centres of secondary lymphoid follicles and requires the enzyme activation-induced cytidine deaminase (AID) and interactions with other immune cells.
The ability to change the isotype of antibody produced (class switching) by a B cell also occurs in germinal centres and requires AID.
In a secondary response to the same antigen, memory cells are rapidly activated. This process is quicker and more effective than the primary response.
Keywords:
antigens;
memory cells;
clonal expansion;
germinal centres;
affinity maturation;
class switching
[1]
Jason G. Cyster,et al.
Imaging of Germinal Center Selection Events During Affinity Maturation
,
2007,
Science.
[2]
S. Tangye,et al.
Memory B cells: Effectors of long‐lived immune responses
,
2009,
European journal of immunology.
[3]
Antonio Lanzavecchia,et al.
Antigen dependent and independent mechanisms that sustain serum antibody levels.
,
2003,
Vaccine.
[4]
S. Jameson,et al.
Diversity in T cell memory: an embarrassment of riches.
,
2009,
Immunity.
[5]
L. McHeyzer-Williams,et al.
Antigen-specific memory B cell development.
,
2005,
Annual review of immunology.
[6]
K. Rajewsky,et al.
Memory B-cell persistence is independent of persisting immunizing antigen
,
2000,
Nature.
[7]
Andreas Radbruch,et al.
Maintenance of serum antibody levels.
,
2005,
Annual review of immunology.
[8]
J. Altman,et al.
Virus-specific CD8+ T cells in primary and secondary influenza pneumonia.
,
1998,
Immunity.
[9]
R. Germain,et al.
Optimal germinal center responses require a multistage T cell:B cell adhesion process involving integrins, SLAM-associated protein, and CD84.
,
2010,
Immunity.
[10]
F. Papavasiliou,et al.
A coming-of-age story: activation-induced cytidine deaminase turns 10
,
2009,
Nature Immunology.
[11]
Antonio Lanzavecchia,et al.
Understanding the generation and function of memory T cell subsets.
,
2005,
Current opinion in immunology.
[12]
Facundo D Batista,et al.
Early events in B cell activation.
,
2010,
Annual review of immunology.
[13]
P. Reichardt,et al.
APC, T cells, and the immune synapse.
,
2010,
Current topics in microbiology and immunology.