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INMUNOLOGIA MOLECULAR
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Page 1: INMUNOLOGIA MOLECULAR I.ppt [Sólo lectura] · Pathways of differentiation of a pluripotent hematopoietic stem cell of the bone marrow 136380 differentiate in the thymus differentiate

INMUNOLOGIA MOLECULAR

Page 2: INMUNOLOGIA MOLECULAR I.ppt [Sólo lectura] · Pathways of differentiation of a pluripotent hematopoietic stem cell of the bone marrow 136380 differentiate in the thymus differentiate

HUMORAL CELULAR

INMUNIDAD IgM MacrófagosNATURAL Células NK

(sin memoria) Neutrófilos

INMUNIDAD IgG Linfocitos CD4+ ADAPTATIVA (helper)(con memoria) Linfocitos CD8+ (CTL)

JM/03Medicina Molecular

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Pathways of differentiation of a pluripotenthematopoietic stem cell of the bone marrow

136380

differentiate in the thymus

differentiate in the bone marrow

Stemcells

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ANTIGENOS

Moléculas reconocidas por receptores en células B (B cellreceptor) o T (T cell receptor).

Hapteno : antígeno que para ser reconocido debe ser unido a un

carrier (hidratos de carbono)

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How many environmental antigens are we exposed to

during our lifetime?

The immune system responds to hundreds of thousands of foreign antigens introduced from the environment

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Examples of antigen, immunogen and epitopes

Antigen

Epitope A Epitope B

Immunogen

Epitope B

Antibody A Antibody B

Antibody B

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ANTICUERPOS

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RECEPTORES ANTIGENICOS

• B cell receptor (linfocitos B) = reconoce Ag nativo

• T cell receptor (linfocitos T) = reconoce Ag procesado

JM/00Medicina Molecular

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ANTIGENO CON MULTIPLES EPITOPES

SUERO CON MULTIPLES ANTICUERPOS

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APCB Ab

CD4

CD8

Ag

Ag Processing

HelpHelp

1. 2.

The Immune Response:

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LINFOCITO CD4 ACTIVADO

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Role of T-Helper cells in antibody formation.

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LINFOCITO B EN REPOSO

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LINFOBLASTOS B

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Lymph node

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Germinal center in lymph node

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PLASMOCITO

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PLASMOCITO APOPTOTICO

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Primary and secondary antibody responses.

136384

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¿Cómo se produce la gran diversidad de anticuerpos?

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Susumu TonegawaPremio Nobel 1987

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Producción de cadena κ

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GENES CODIFICANTES PARA INMUNOGLOBULINAS

• Cluster IGH: cadena H; crom.14;V,D,J,C.

• Cluster IGK: cadena K; crom.2; V,J,C.

• Cluster IGL(λ): cadena λ; crom. 22; V,J,C.

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ANTICUERPOS MONOCLONALES

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b. 1927(in Bahia Blanca, Argentina)d. 2002

b. 1946d. 1995

b. 1911d. 1994

MRC Laboratory of Molecular BiologyCambridge, United Kingdom

Basel Institute for ImmunologyBasel, Switzerland

Basel Institute for ImmunologyBasel, Switzerland

Argentina and United KingdomFederal Republic of GermanyDenmark

1/3 of the prize1/3 of the prize1/3 of the prize

César MilsteinGeorges J.F. KöhlerNiels K. Jerne

Find a Laureate:

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• antibodies produced by differentiated B-cells

• recombination results in B-cell lineages producing distinct antibodies

• serum contains antibodies representing many lineages

• difficult to isolate B-cells of defined specificity

• cannot grow B-cells in culture

Kohler and Milstein (1975)

• fused B-cells with myelomacells stable hybridoma

• hybridoma secretes monoclonal antibody

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• immunized mouse making desired antibodies

• boost 3-4 days before fusion• remove spleen and harvest

cells• mix with myeloma cells in

presence of fusogenic agent

Balb/c Mouse

MOPC 21 (tumor)

P3K (cell line)

P3-X63Ag8 (HGPRT-)

X63-Ag8.653 (IgG-)

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HGPRT = hypoxanthine-guanine phosphoribosyl transferaseDHFR = dihydrofolate reductase

HAT Medium:• Hypoxanthine

(purine salvage)• Aminopterin

(DHFR inhibitor)• Thymidine

(pyrimidine salvage)

Nucleotide Metabolism:

• salvage and de novo pathways

• HGPRT essential for purine salvage

• DHFR essential for de novo synthesis

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Selection in HAT Medium

Human mAbs produced by trans-forming lymphocytes with EBV

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Cloning Methods•soft agar• limiting dilution

Screening/Cloning

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• produce mAbs in vitro or with ascites

• harvest culture media (supernatant)– in vitro material is less

concentrated and contains bovine serum

• ascites are tumors grown in peritoneal cavity– ascites fluid and sera

contain high [mAb]– minor contamination

with mouse IgG

Production

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HAMA ("human anti-mouse antibodies"). HAMA ("human anti-mouse antibodies").

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Mouse monoclonal antibodies have been genetically engineered to replace all of the antibody molecule with human counterparts except the hypervariableregions directly involved with antigen binding.Humanized monoclonal antibodies are

currently be tested in human clinical trials.

Humanized Monoclonal Antibodies

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RECEPTORES ANTIGENICOS

• T cell receptor (linfocitos T) = reconoce Agprocesado

• B cell receptor (linfocitos B) = reconoce Agnativo

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MECANISMO DE ACCION DE LOS ANTICUERPOS

Via ComplementoADCC (antibody-dependent-

cellular-cytotoxicity

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• COMPLEMENTO

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MAC (complejo ataque complemento)


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