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Blood and Immunity Physiology
Laboratory Session
Day1
1. Total WBC count
2. RBC count
3. Differential WBC count
1.Total white blood cell count
Significance of the test
• To investigate infections and unexplained
fever.
• To monitor treatments which can cause
leucopenia.
• To diagnose leukemia.
Principle of the test
• Whole blood is diluted 1:20 in weak acetic
acid solution which lyses red blood cells but
preserves leukocytes to be counted.
• The count is multiplied by dilution factor and
volume correction factor .
• The number of WBC is reported as number of
cells per microliter(µl) of whole blood.
Specimen
• EDTA anticoagulated blood or Capillary blood
can be used for counting WBC
Materials and Reagents
• Hemocytometer(improved neubauer chamber)
• WBc thoma pippet
• Diluting fluid(weak acetic acid)
• Cover glass
• Cotton
• Microscope
• alcohol
Cont’d….
WBC Thoma Pippet
Procedure
1.Mix the anticoagulated blood carefully
2.Suck the blood into WBC thoma pipette
exactly up to 0.5 mark.
3.Wipe the excess blood outside the pipete using
cotton
4.Take diluting fluid up to 11 mark
5.Gently rotate the pipette for mixing
6.Discard the first drops of unmixed solution
present at the stem of the pipette
Cont’d…..
7.Charge the counting chamber and allow 2
minutes for settling of cells
8.Count white cells in the four corner squares of
the haemocytometer using microscope.
About the haemocytometer
• The chamber has 9 large
squares
• Each square is 1mmx1mm
(area 1mm2
)and 0.1mm depth
(volume 0.1mm3
)
• WBC is count in the four
large Corner squares
• Volume used for counting
WBC is 4x0.1mm=0.4mm3
Calculation
• The dilution and the volume used must be corrected.
• The dilution is corrected by dilution correction factor(DCF)
• The volume is corrected by volume correction factor(VCF)
Total WBC Count = no of cell counted x DCF x VCF
DCF =20(1:20)
VCF =Volume desired/volume used
1mm3
/0.4mm3
= 2.5
WBC count =no of cell counted x20x2.5
= no of cell counted x50/µl
Normal range : 4,000-10,000/µl (4 - 10 x10 3
/µl)
Interpretation
• Increase in
Acute infection eg pneumonia,tonsilitis
 Inflammation and tissue necrosis
eg burn,Arthritis
Leukemia and myloproliferetive disorders
Stress
Strenuous exercise
Cont’d….
• Decrease in
Viral and parasitic infections
Drugs and reaction to chemicals
Hypresplenism
Aplastic anemia etc…
2.Red blood cell count
Significant of the test
• Used to diagnose and classify anemia.
• To calculate red cell indices
Principle of the test
• Whole blood is diluted 1:200 in hayem’s
solution which maintains the disc like shape
of red cells and prevents agglutination.
• RBCs are counted under microscope
• The count is multiplied by dilution factor and
volume correction factor
• The number of RBC is reported as number of
cells per microliter(µl) of whole blood
Specimen
• EDTA anticoagulated blood or capillary blood
can be used for counting RBC
Material and reagents
• Haemocytometer
• RBC thoma pippet
• Cover glass
• Diluting fluid (hayem’s solution)
• Microscope
• Cotton
• alcohol
Procedure
1.Mix the anticoagulated blood carefully
2.Suck the blood into pipette exactly up to 0.5 mark.
3.Wipe the excess blood outside the pipete using
cotton
4.Take diluting fluid up to 101 mark
5.Gently rotate the pipette for mixing
6.Discard the first drops of unmixed hayem’s
solution present at the stem of the pipette
Cont’d….
7.Charge the counting chamber and allow 2
minutes for settling of cells
8.Count red cells in the central 5 small squares of
the haemocytometer using microscope
About the haemocytometer
• RBC counts in the central large
square(1mmx1mm)
• The central large square is divided
in to 25 smaller squares
• RBC is counted in the 5 out of these
25 smaller squares
• Each smaller square is
1/25(0.04mm3
)and its volume is
0.004mm3
• So volume used for RBC count is
5x0.004mm3
= 0.02mm3
Calculation
RBC Count = no of cell counted x DCFxVCF
DCF = 200(1:200)
VCF=volume desired/volume used
= 1cumm/0.02cumm=50
RBC count = no of cell counted x200x50
= no of cell counted x10,000/µl
Normal range
Adult male 5-6x10^6/µl
adult female 4- 5x10^6/µl
Interpretation
 RBC count increases in
 Polycythemia Vera
 Conditions that result in low oxygen(heart
failure,COPD,pulmonary fibrosis, high altitude)
 Kidney cancers
 Dehydration
RBC count decreases in
Anemia
 Sever falciparum parasitic infection
 Blood loss
3 Differential WBC count
Significance of the test
 To help determine the cause of abnormal results on a WBC
count.
 To diagnose or monitor an illness affecting the immune
system.
Principle
• Blood film is prepared then allow to air dry.
• The dried smear stains with Romanowsky stains (giemsa
or wright stain).
• Cells will be counted
• Then the percent distribution of each cell is calculated
Morphology of different leukocytes
• Leukocytes differ in
Their size
Shape of nucleus
Color of cytoplasm
Presence/absence of granules in cytoplasm
Color of granules
cont’d
Segmented neutrophil
• Size: 12-15µm
• Nucleus: segmented
with 3-5 lobes
• Cytoplasm : pale
staining with small
neutrophilic granules
• Segmented neutrophil
Cont’d….
 lymphocyte
Small lymphocyte
• Size :10-12µm
• Nucleus: dark round
• cytoplasm:blue
Large lymphocyte
• Size : 12-16µm
• Nucleus : round , oval
or indented
• Cytoplasm :blue
Cont’d…….
Monocyte
• Size :15-20 µm
• Nucleus: round
,indented or folded
monocyte
Eosinophil
• Size: 12-17µm
• Nucleus : bilobed
• Cytoplasm :pale staining
with orange red granules
Eosinophil
Contd…..
 Basophil
• Size: 10-12µm
• Nucleus: bilobed but usually
obscured by granules
• large blue-violet granules in
the cytoplasm
Basophil
• The are two types of counting
1 Relative count: is the simple percentage distribution
of white blood cells.
2 Absolute count: is the exact count of leukocytes in
the peripheral blood.
Absolute count = relative count X total leukocyte
count.
Cont’d…..
Differential WBC reference range
Adults
Neutrophils …………… 2.0 – 7.5 × 10^9/l (40 – 75%)
Lymphocytes ………….1.2 – 4.0 × 10^9/l (21 – 40%)
Monocytes …………….0.2 – 1.0 × 10^9/l (2-10%)
Eosinophils …..………. 0.02 - 0.6 × 10^9/l (1-6%)
Basophils …..………… 0.01 – 0.1 × 10^9/l (0-1%)
Interpretation
Neutrophilia
• It is caused by:
 Acute bacterial infections
Physical and emotional stress
 Tissue destruction or necrosis
Myeloid leukomia
Cont’d…..
Neutropenia:
It is caused by:
Bone marrow failure
 Myeloid hypoplasia
 Drugs (chloramphenicol, phenylbutazone)
Ionizing radiation
Cont’d…..
Eosinophilia:
it Occurs during:
 Allergic diseases: bronchial asthma
 Intestinal parasitic infections
Basophilia:
Some allergic reactions
Chronic myelogenous leukemia(CML)
Cont’d…..
Monocytosis
• Chronic bacterial infections, e.g. tuberculosis,
typhoid, bacterial endocarditis
• Chronic myelomonocytic leukaemia
Cont’d…..
Lymphocytosis:
occurs during
• Infections in children, e.g. whooping cough,
mumps, measles, chicken pox
• viral infections: Epstein-Barr virus
,cytomegalovirus,
• Acute and chronic lymphocytic leukemia
Cont’d
Lymphocytopenia
 Immune deficiency disorders: HIV/AIDS
 Drugs, radiation therapy

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Blood and Immunity physiology prepared by Kiflay Mulugeta

  • 1. Blood and Immunity Physiology Laboratory Session Day1 1. Total WBC count 2. RBC count 3. Differential WBC count
  • 2. 1.Total white blood cell count Significance of the test • To investigate infections and unexplained fever. • To monitor treatments which can cause leucopenia. • To diagnose leukemia.
  • 3. Principle of the test • Whole blood is diluted 1:20 in weak acetic acid solution which lyses red blood cells but preserves leukocytes to be counted. • The count is multiplied by dilution factor and volume correction factor . • The number of WBC is reported as number of cells per microliter(µl) of whole blood.
  • 4. Specimen • EDTA anticoagulated blood or Capillary blood can be used for counting WBC
  • 5. Materials and Reagents • Hemocytometer(improved neubauer chamber) • WBc thoma pippet • Diluting fluid(weak acetic acid) • Cover glass • Cotton • Microscope • alcohol
  • 8. Procedure 1.Mix the anticoagulated blood carefully 2.Suck the blood into WBC thoma pipette exactly up to 0.5 mark. 3.Wipe the excess blood outside the pipete using cotton 4.Take diluting fluid up to 11 mark 5.Gently rotate the pipette for mixing 6.Discard the first drops of unmixed solution present at the stem of the pipette
  • 9. Cont’d….. 7.Charge the counting chamber and allow 2 minutes for settling of cells 8.Count white cells in the four corner squares of the haemocytometer using microscope.
  • 10. About the haemocytometer • The chamber has 9 large squares • Each square is 1mmx1mm (area 1mm2 )and 0.1mm depth (volume 0.1mm3 ) • WBC is count in the four large Corner squares • Volume used for counting WBC is 4x0.1mm=0.4mm3
  • 11.
  • 12. Calculation • The dilution and the volume used must be corrected. • The dilution is corrected by dilution correction factor(DCF) • The volume is corrected by volume correction factor(VCF) Total WBC Count = no of cell counted x DCF x VCF DCF =20(1:20) VCF =Volume desired/volume used 1mm3 /0.4mm3 = 2.5 WBC count =no of cell counted x20x2.5 = no of cell counted x50/µl Normal range : 4,000-10,000/µl (4 - 10 x10 3 /µl)
  • 13. Interpretation • Increase in Acute infection eg pneumonia,tonsilitis  Inflammation and tissue necrosis eg burn,Arthritis Leukemia and myloproliferetive disorders Stress Strenuous exercise
  • 14. Cont’d…. • Decrease in Viral and parasitic infections Drugs and reaction to chemicals Hypresplenism Aplastic anemia etc…
  • 15. 2.Red blood cell count Significant of the test • Used to diagnose and classify anemia. • To calculate red cell indices
  • 16. Principle of the test • Whole blood is diluted 1:200 in hayem’s solution which maintains the disc like shape of red cells and prevents agglutination. • RBCs are counted under microscope • The count is multiplied by dilution factor and volume correction factor • The number of RBC is reported as number of cells per microliter(µl) of whole blood
  • 17. Specimen • EDTA anticoagulated blood or capillary blood can be used for counting RBC
  • 18. Material and reagents • Haemocytometer • RBC thoma pippet • Cover glass • Diluting fluid (hayem’s solution) • Microscope • Cotton • alcohol
  • 19. Procedure 1.Mix the anticoagulated blood carefully 2.Suck the blood into pipette exactly up to 0.5 mark. 3.Wipe the excess blood outside the pipete using cotton 4.Take diluting fluid up to 101 mark 5.Gently rotate the pipette for mixing 6.Discard the first drops of unmixed hayem’s solution present at the stem of the pipette
  • 20. Cont’d…. 7.Charge the counting chamber and allow 2 minutes for settling of cells 8.Count red cells in the central 5 small squares of the haemocytometer using microscope
  • 21. About the haemocytometer • RBC counts in the central large square(1mmx1mm) • The central large square is divided in to 25 smaller squares • RBC is counted in the 5 out of these 25 smaller squares • Each smaller square is 1/25(0.04mm3 )and its volume is 0.004mm3 • So volume used for RBC count is 5x0.004mm3 = 0.02mm3
  • 22. Calculation RBC Count = no of cell counted x DCFxVCF DCF = 200(1:200) VCF=volume desired/volume used = 1cumm/0.02cumm=50 RBC count = no of cell counted x200x50 = no of cell counted x10,000/µl Normal range Adult male 5-6x10^6/µl adult female 4- 5x10^6/µl
  • 23. Interpretation  RBC count increases in  Polycythemia Vera  Conditions that result in low oxygen(heart failure,COPD,pulmonary fibrosis, high altitude)  Kidney cancers  Dehydration RBC count decreases in Anemia  Sever falciparum parasitic infection  Blood loss
  • 24. 3 Differential WBC count Significance of the test  To help determine the cause of abnormal results on a WBC count.  To diagnose or monitor an illness affecting the immune system. Principle • Blood film is prepared then allow to air dry. • The dried smear stains with Romanowsky stains (giemsa or wright stain). • Cells will be counted • Then the percent distribution of each cell is calculated
  • 25. Morphology of different leukocytes • Leukocytes differ in Their size Shape of nucleus Color of cytoplasm Presence/absence of granules in cytoplasm Color of granules
  • 26. cont’d Segmented neutrophil • Size: 12-15µm • Nucleus: segmented with 3-5 lobes • Cytoplasm : pale staining with small neutrophilic granules • Segmented neutrophil
  • 27. Cont’d….  lymphocyte Small lymphocyte • Size :10-12µm • Nucleus: dark round • cytoplasm:blue Large lymphocyte • Size : 12-16µm • Nucleus : round , oval or indented • Cytoplasm :blue
  • 28. Cont’d……. Monocyte • Size :15-20 µm • Nucleus: round ,indented or folded monocyte
  • 29. Eosinophil • Size: 12-17µm • Nucleus : bilobed • Cytoplasm :pale staining with orange red granules Eosinophil
  • 30. Contd…..  Basophil • Size: 10-12µm • Nucleus: bilobed but usually obscured by granules • large blue-violet granules in the cytoplasm Basophil
  • 31. • The are two types of counting 1 Relative count: is the simple percentage distribution of white blood cells. 2 Absolute count: is the exact count of leukocytes in the peripheral blood. Absolute count = relative count X total leukocyte count.
  • 32. Cont’d….. Differential WBC reference range Adults Neutrophils …………… 2.0 – 7.5 × 10^9/l (40 – 75%) Lymphocytes ………….1.2 – 4.0 × 10^9/l (21 – 40%) Monocytes …………….0.2 – 1.0 × 10^9/l (2-10%) Eosinophils …..………. 0.02 - 0.6 × 10^9/l (1-6%) Basophils …..………… 0.01 – 0.1 × 10^9/l (0-1%)
  • 33. Interpretation Neutrophilia • It is caused by:  Acute bacterial infections Physical and emotional stress  Tissue destruction or necrosis Myeloid leukomia
  • 34. Cont’d….. Neutropenia: It is caused by: Bone marrow failure  Myeloid hypoplasia  Drugs (chloramphenicol, phenylbutazone) Ionizing radiation
  • 35. Cont’d….. Eosinophilia: it Occurs during:  Allergic diseases: bronchial asthma  Intestinal parasitic infections Basophilia: Some allergic reactions Chronic myelogenous leukemia(CML)
  • 36. Cont’d….. Monocytosis • Chronic bacterial infections, e.g. tuberculosis, typhoid, bacterial endocarditis • Chronic myelomonocytic leukaemia
  • 37. Cont’d….. Lymphocytosis: occurs during • Infections in children, e.g. whooping cough, mumps, measles, chicken pox • viral infections: Epstein-Barr virus ,cytomegalovirus, • Acute and chronic lymphocytic leukemia
  • 38. Cont’d Lymphocytopenia  Immune deficiency disorders: HIV/AIDS  Drugs, radiation therapy

Notas del editor

  1. A differential WBC count provide information on the different white cells present in the circulating blood White blood cells are grouped in to two i.e granulocytes(with granules) and agranulocytes(with out granules) Granulocytes are neutrophil , eosinophil and basophil. Agranulocytes are lymphocyte and monocyte.