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MiHA 496 Miller–Fisher syndrome (MFS)<br />

Peter Miescher.<br />

Live cells<br />

lymphokine-activated macrophages. IFN-γ can induce macrophages<br />

to express the MIG gene. Tissue sources include<br />

lymphokine-activated macrophages, IFN-γ-treated human<br />

peripheral blood monocytes, and IFN-γ-treated human<br />

monocytic cell line THP-1. Target cells include human<br />

tumor-infiltrating lymphocytes (TILs) and monocytes.<br />

MiHA<br />

Refer to minor histocompatibility antigens.<br />

MIICs<br />

MHC class compartments or class II vesicles. These<br />

specialized late endosomal spaces comprise a segment<br />

of the exogenous (endocytic) antigen processing pathway.<br />

Endolysosomal MHC-CLIP complexes enter MIICs where<br />

CLIP exchange and peptide loading occur.<br />

Mikulicz’s syndrome<br />

Lymphocytic inflammation in the parotid gland. This condition<br />

represents a type of Sjögren’s syndrome.<br />

Milgrom, Felix (1919–2007)<br />

Polish-American investigator who worked at the University<br />

of Buffalo in New York State. He and Ernest Witebsky<br />

described anti-immunoglobulin antibodies. They immunized<br />

rabbits with aggregated autologous globulin and<br />

discovered that the rabbits produced antibodies with greater<br />

reactivity for human globulin than for rabbit globulin.<br />

Miller, J.F.A.P. (1931–)<br />

Proved the role of the thymus in immunity while investigating<br />

Gross’ leukemia in neonatal mice.<br />

Miller–Fisher syndrome (MFS)<br />

A variant of Guillain–Barré syndrome (GBS) that has a<br />

subacute onset and follows infectious illnesses of which<br />

Live cells Dead cells All cells dead<br />

Microlymphocytotoxicity.<br />

Felix Milgrom.<br />

J.F.A.P. Miller.<br />

Campylobacter jejuni infection is the most common. Fewer<br />

than 5% of GBS cases have MFS. Clinically, MFS presents<br />

as ophthalmoplegia, ataxia, and areflexia. The extremity and<br />

trunk muscles exhibit little or no weakness. The spinal fluid<br />

protein is seldom increased, and nerve conduction studies are<br />

usually normal. Most MFS patients have circulating polyclonal<br />

antibodies to GQb1 ganglioside, a minor ganglioside component<br />

of both the central and peripheral nervous systems. These<br />

antibodies are highest initially and fall with recovery.

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