Body Fluids & Circulation – Blood Groups, Rh Factor & Erythroblastosis Foetalis (Lecture 04)
Composition of Blood
- Blood = Plasma + Formed elements (RBC, WBC, platelets)
- Plasma (~55% of blood volume)
- ≈90% water; ≈7% proteins; ≈0.9% salts; rest = nutrients, hormones, gases, wastes.
- Major plasma proteins (all circulating in inactive form)
- Albumins → osmotic balance
- Globulins → antibodies
- Fibrinogen & prothrombin → clotting factors
- Serum
- Plasma − (fibrinogen + clotting factors)
- Cannot undergo coagulation ➜ diagnostic use.
- Formed elements (~45%)
- Erythrocytes: ≈4.5–5.5×106/mm3
- Leukocytes: ≈6–8×103/mm3
- Thrombocytes (platelets): ≈1.5–3.5×105/mm3
Blood Coagulation (Clotting Cascade)
- Trigger: Injury damages endothelium ➜ tissue factor + platelet factors released.
- Key sequential conversions
- Prothrombin (inactive)ThrombokinaseCa2+Thrombin (active)
- Fibrinogen (soluble)ThrombinFibrin (insoluble threads)
- Fibrin network + trapped formed elements = clot (dark reddish-brown scab)
- Platelets provide phospholipids & serotonin (vasoconstriction).
- Vitamin K essential for hepatic synthesis of several factors.
- Delayed clotting → common causes
- Thrombocytopenia (↓ platelets)
- Defect in Castle’s intrinsic factor ➜ ↓ vitamin B12 ➜ faulty prothrombin synthesis
- Folic-acid malabsorption
White Blood Cells & Their Special Roles
- Neutrophils (50–70%) ➜ phagocytosis of microbes.
- Basophils (0.5–1%) ➜ release histamine, serotonin, heparin ➜ inflammatory & allergic reactions.
- Eosinophils (1–4%) ➜ combat parasites, modulate allergy (diagram in lecture; MCQ answer = eosinophil).
- Monocytes & lymphocytes ➜ immunity.
ABO Blood-Group System
- Based on two RBC surface antigens (agglutinogens) A & B.
- Plasma carries natural antibodies (agglutinins) formed without prior sensitisation.
| Blood-group | Antigen(s) on RBC | Antibody in plasma | Compatible donor(s) |
|---|
| A | A | anti-B | A, O |
| B | B | anti-A | B, O |
| AB | A & B | nil | AB, A, B, O |
| O | nil | anti-A & anti-B | O |
- Consequences
- Group O = “universal donor” (no antigens to attack).
- Group AB = “universal recipient” (no antibodies).
- Transfusion rule: Match both antigen & antibody landscape to avoid haemolytic transfusion reactions (agglutination ↓ RBC → renal failure, death).
Rh (Rhesus) Blood-Group System
- Rh antigen (D-factor) present in ≈80% humans ➜ Rh+. Absence ➜ Rh−.
- Unlike ABO, Rh antibodies are not natural; they are produced only after exposure to Rh+ RBCs (transfusion or feto-maternal bleed).
- Before transfusion ➜ cross-match for Rh as well.
Erythroblastosis Foetalis (Haemolytic Disease of the New-Born, HDN)
- Pathogenesis sequence
- Mother Rh− × Father Rh+ → Foetus Rh+.
- First pregnancy: placental barrier prevents mixing; no problem.
- At delivery #1 some foetal Rh+ RBCs enter maternal circulation.
- Mother’s immune system produces anti-Rh (IgG) antibodies (memory cells stored).
- Second & subsequent Rh+ pregnancies: IgG crosses placenta (tiny size) ➜ bind foetal RBC ➜ agglutination & haemolysis.
- Clinical features in foetus/new-born
- Severe anaemia (↓ RBC, ↓ Hb)
- Jaundice (↑ bilirubin & biliverdin from haem breakdown)
- Hepatosplenomegaly, oedema (hydrops foetalis), possible intra-uterine or neonatal death.
- Prevention – Rhogam Protocol
- Immediately (<72 h) after 1st delivery/abortion/amniocentesis, inject mother with anti-Rh γ-globulin (Rhogam).
- Rhogam binds & destroys any foetal Rh+ RBCs before mother is sensitised.
- No immunological memory from Rhogam itself.
Lymph (brief touch, as per topic list)
- Ultrafiltrate of blood plasma; found in lymphatic vessels.
- Functions: returns interstitial fluid & proteins to blood, transports fats (lacteals), lymphocytes circulation, maintains tissue fluid balance.
Key MCQ / Assertion–Reason Points Discussed in Lecture
- Plasma + formed elements constitute blood; serum cannot clot → BOTH TRUE.
- "Fibrinogens, prothrombins are in active state" (F) & "fibrinogens themselves form clot mesh" (F) → BOTH FALSE.
- Thrombin converts inactive fibrinogen to fibrin (answer: Fibrin).
- Basophils cause inflammatory reactions via histamine/serotonin (answer: Basophils).
- Injury triggers platelet/tissue factors → activates clotting; Reason correctly explains Assertion (A-type correct explanation).
- Dark scab = fibrin network with trapped cells; both descriptive statements correct.
- Diagram identification (3) Eosinophil – associated with allergy.
- Erythroblastosis foetalis occurs in 2nd pregnancy; problem absent if foetus Rh− → BOTH STATEMENTS CORRECT.
- Correct set about blood groups → I, II, V (O has both antibodies; B→A transfusion incompatible; anti-Rh after first child) .
- ABO donor-compatibility figure: correct option (c) (AB receives from all, O donates to all).
- Excessive bleeding delay → Thrombocytopenia (low platelets) probable cause.
Real-World & Clinical Significance
- Mandatory blood-group & Rh typing in blood banks, prenatal care, emergency transfusions.
- Universal donor/recipient concept simplifies mass-casualty triage.
- Rhogam availability has drastically reduced HDN incidence worldwide.
- Basophil-mediated inflammatory response forms basis for antihistamine therapy.
- Understanding cascade exploited pharmaceutically: anticoagulants (heparin, warfarin), fibrinolytics (streptokinase) in thrombosis management.
Ethical / Philosophical Angle
- Prenatal testing & Rh prophylaxis highlight preventive medicine ethics – treat mother to protect an unborn child.
- Blood donation campaigns rely on public altruism; universal donor group "O" individuals carry special responsibility.
Rapid-Revision Flash Facts
- O = universal donor; AB = universal recipient.
- Rh antigen present in ≈80% population.
- Rh antibodies are IgG; can cross placenta.
- Rhogam: passive immunisation, no memory.
- Coagulation key ions: Ca2+ and vitamin K.
- Basophil → histamine; Eosinophil → anti-parasitic + allergy; Neutrophil → phagocyte.
- Serum = plasma – clotting factors ➜ used in diagnostics & antiserum production.