You are currently viewing 45 Difference Between Immunoglobulins and Complement Proteins

45 Difference Between Immunoglobulins and Complement Proteins

A vital part of the immune system, immunoglobulins and complement proteins have different functions in protecting the body from infections and sustaining immunological responses. 

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

Lyses microbes and triggers inflammation

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.

Team Serology Test

Hi, I'm the Founder and Developer of the Serology Test, a blog truly devoted to Medics. I am a Medical Lab Tech, a Web Developer and Bibliophiliac. My greatest hobby is to teach and motivate other peoples to do whatever they wanna do in life.

Leave a Reply