A vital part of the immune system, immunoglobulins and complement proteins have different functions in protecting the body from infections and sustaining immunological responses.Â
B lymphocytes (B cells) create the specialized proteins known as immunoglobulins (Ig), also referred to as antibodies, in reaction to the presence of foreign substances such as antigens. Four protein chains, two identical heavy chains and two identical light chains, make up the Y-shaped structure of antibodies. The Y-shaped antibody molecule has a region on each arm that can recognise and bind to a particular antigen.
Immunoglobulins fall into five basic categories, each with a distinct set of properties:
- The first antibody to be produced in response to an infection is IgM. It is essential for the pathogens to agglutinate (clump) and for the complement system to be activated.
- IgG: The most prevalent class of antibodies, IgG protects babies by neutralizing pathogens, encouraging phagocytosis (the immune system’s devouring of pathogens), and facilitating transit across the placenta.
- IgA: Predominantly present in physiological fluids including saliva, tears, and mucous secretions, IgA offers localized immunity on mucosal surfaces and keeps infections out of the body.
- IgE: This group of antibodies is linked to allergic reactions and parasite defense. Allergy symptoms are brought on by IgE, which causes mast cells to produce histamine.
- IgD: Although its precise role in B cell activation is not fully understood, IgD can be located on their surface.
Over 30 proteins make up the complement system, which collaborates to strengthen the immune response to infections. Both the innate and the adaptive immune systems contain complement proteins, which have a variety of functions.
Complement proteins can coat infections with chemicals that promote phagocytosis, a process known as poisoning. Opsonization is the process that makes it simpler for immune cells to detect and absorb viruses.
- Complement activation causes the release of inflammatory mediators such as cytokines, which draw immune cells to the infection site and cause inflammation.
- Cell lysis: Complement proteins can assemble into a membrane attack complex (MAC), which breaks pores in pathogens’ membranes and kills them.
- Immune complexes (antigen-antibody complexes) are cleared from circulation with the help of complement proteins.
- Enhancement of Adaptive Immune Response: Complement activation can also help to activate B cells and increase the generation of antibodies.
S.No. |
Aspects |
Immunoglobulins |
Complement Proteins |
1 |
Definition |
Antibodies produced by B cells |
Serum proteins in the immune system |
2 |
Classification |
IgG, IgM, IgA, IgD, IgE |
C1-C9, factors B, D, P, H, and I |
3 |
Synthesis Location |
Mainly in plasma cells |
Various cell types, mainly liver |
4 |
Structure |
Y-shaped with heavy and light chains |
Composed of multiple proteins |
5 |
Antigen Recognition |
Bind directly to antigens |
Do not directly bind antigens |
6 |
Specificity |
Highly specific to antigens |
Non-specific activation |
7 |
Effector Functions |
Opsonization, neutralization, complement activation |
Complement cascade activation |
8 |
Molecular Weight |
Smaller, around 150 kDa |
Larger, varying from 25 kDa to 200 kDa |
9 |
Role in Immunity |
Adaptive immune response |
Part of innate immune response |
10 |
Presence in Serum |
Present as soluble proteins |
Present as soluble proteins |
11 |
Antibody Classes |
IgG, IgM, IgA, IgD, IgE |
C1q, C1r, C1s, C2, C3, C4, C5, C6, C7, C8, C9 |
12 |
Activation |
Antigen binding activates them |
Activation by enzymatic cascades |
13 |
Antigen Binding Sites |
Variable and constant regions |
No antigen-binding sites |
14 |
Secretion |
Secreted by plasma cells |
Synthesized by liver and other cells |
15 |
Half-life |
Longer half-life (days to weeks) |
Shorter half-life (hours to days) |
16 |
Opsonization |
Yes |
No |
17 |
Effector Enzymes |
No |
Yes (e.g., C3 convertase) |
18 |
Receptors |
Fc receptors on immune cells |
Receptors on various cell types |
19 |
Memory |
Contribute to immunological memory |
No memory function |
20 |
Primary Function |
Adaptive immune response |
Enhance immune responses |
21 |
Clonal Selection |
Involved in clonal selection |
Not involved in clonal selection |
22 |
Secretion Regulation |
Regulated by B cell activation |
Constitutive secretion |
23 |
Role in Autoimmunity |
Can contribute to autoimmune diseases |
Not directly implicated in autoimmunity |
24 |
Diversity |
High diversity due to variable regions |
Limited diversity |
25 |
Isotypes |
Different isotypes (IgG1, IgG2, etc.) |
Different factors (C1, C2, etc.) |
26 |
Activation Trigger |
Antigen recognition |
Pathogen surface components |
27 |
Opsonization Mechanism |
Coating pathogens with antibodies |
No opsonization |
28 |
Crosslinking |
Can crosslink antigens |
No crosslinking |
29 |
Role in Humoral Immunity |
Central to humoral immunity |
Enhance humoral immunity |
30 |
Role in Cell Lysis |
Limited role in cell lysis |
Crucial in cell lysis |
31 |
Role in Inflammation |
Limited role in inflammation |
Can contribute to inflammation |
32 |
Role in Immune Complexes |
Form immune complexes |
Not involved in immune complexes |
33 |
Complement Activation Pathway |
Not involved in complement activation |
Initiates complement cascade |
34 |
Antigen Recognition Timing |
Slower recognition of antigens |
Rapid recognition of pathogens |
35 |
Role in Allergic Reactions |
Can trigger allergic reactions |
Not involved in allergies |
36 |
Role in Phagocytosis |
Enhances phagocytosis |
No direct role in phagocytosis |
37 |
Antibody Production Regulation |
Regulated by antigen exposure |
Constitutively present |
38 |
Role in Antigen Presentation |
Antigen presentation via MHC |
No role in antigen presentation |
39 |
Role in Immune Memory |
Essential for immune memory |
No role in immune memory |
40 |
Effect on Microbes |
Neutralizes and opsonizes microbes |
|
41 |
Role in Self vs. Non-self Recognition |
Discriminate between self and non-self |
No role in this discrimination |
42 |
Association with Diseases |
Implicated in autoimmune diseases |
Complement deficiencies lead to infections |
43 |
Activation Mechanism |
Binding to specific antigens |
Activation by proteolytic enzymes |
44 |
Role in Antibody-Mediated Immunity |
Central role in this type of immunity |
No direct role in this type of immunity |
45 |
Role in Adaptive Immune Response |
Key players in adaptive immunity |
Limited involvement in adaptive immunity |
Frequently Asked Questions (FAQs)
Q1.What's an immunoglobulin's structure?
The Y-shaped structure of immunoglobulins is made up of two heavy chains and two light chains. Disulfide bonds hold these chains together. Antigen-binding sites, which are the tips of the Y-shaped structure, are in charge of binding to particular antigens.
Q2.What function do IgG antibodies serve?
The most prevalent and adaptable antibodies are IgG antibodies. By eliminating toxins, boosting phagocytosis, and crossing the placenta to safeguard fetuses, they offer long-lasting protection.
Q3.Describe opsonization?
Complement proteins wrap infections to make them more recognisable to phagocytic cells like macrophages and neutrophils. This process is known as opsonization. As a result, pathogen engulfment and killing are more effective.
Q4.The membrane attack complex (MAC) is what, exactly?
The complement proteins that constitute the membrane assault complex cooperate to puncture the membranes of the target cells, leading to cell lysis.
Q5.Complement proteins: Are they a component of innate or acquired immunity?
Although they can interact with and improve the adaptive immune response as well, complement proteins are largely a component of the innate immune response.