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Research time line.


While MS has been identified as a disease for more than 120 years, for most of those years, MS therapy was based on hunches--without controlled trials that measure effectiveness. And people with MS were subjected to hopelessly ineffective treatments--such as tonsil tonsil

Small mass of lymphoid tissue in the wall of the pharynx. The term usually refers to the palatine tonsils on each side of the oropharynx. They are thought to produce antibodies to help prevent respiratory and digestive tract infection but often become infected
 extraction.

Today, while many questions remain to be answered, MS research has been set free by new biotechnology. Treatments under study are no longer shots in the dark. They have a rationale, supported by painstakingly acquired science on how the human body works at its most fundamental level. Four fields--where knowledge has exploded in the past two decades--are yielding important treatment ideas.

* Cell biology Knowledge of the nature of oligodendrocyte oligodendrocyte /ol·i·go·den·dro·cyte/ (-den´dro-sit) a cell of the oligodendroglia.

ol·i·go·den·dro·cyte
n.
One of the cells comprising the oligodendroglia.
 cells is building. These central nervous system cells manufacture myelin myelin /my·elin/ (mi´e-lin) the lipid-rich substance of the cell membrane of Schwann cells that coils to form the myelin sheath surrounding the axon of myelinated nerve fibers. , the material that is damaged in MS.

* Genetics More than one gene governs susceptibility to MS. The search for these genes is now in progress.

* Immunology Immune reactions appear to be responsible for damage to myelin in MS. How the immune system works in MS is still unfolding...but ways to intervene are now possible.

* Virology A triggering agent has long been suspected in MS. Techniques for finding and identifying virus are now easier and faster than ever before.

1860s to 1910s

SCIENTIFIC UNDERSTANDING

* Microscope used to identify myelin, the nerve fiber insulating material (1860) Scientists learn to grow cells in lab dishes (1910s)

* Laws of genetics, ignored in 1850s, re-examined (1900) Term gone first used (1909)

* First clues to how body fights infection: antibodies found (1889)

* Existence of viruses established (1900s)

* Clinical Care

MS described as a distinct disease (1860)

Tonics and stimulants given, including: gold chloride, zinc sulfate, silver nitrate, strychnine strychnine (strĭk`nĭn), bitter alkaloid drug derived from the seeds of a tree, Strychnos nux-vomica, native to Sri Lanka, Australia, and India. , ergot ergot (ûr`gət), disease of rye and other cereals caused by the fungus Claviceps purpurea. The cottony, matlike body, or mycelium, of the fungus develops in the ovaries of the host plant; it eventually turns into a hard pink or purple , belladonna belladonna (bĕlədŏn`ə) or deadly nightshade, poisonous perennial plant, Atropa belladona, of the nightshade family. , electricity, hydrotherapy hydrotherapy, use of water in the treatment of illness or injury. Although the medicinal and hygienic value of water was recognized by the early Greeks, hydrotherapy attained its widest use in the 18th and 19th cent.  

No lasting benefits, no controlled studies

1920s to 1940s

SCIENTIFIC UNDERSTANDING

* Oligodendrocytes (0Iigo's)identified as source of myelin (1928)

Nerve fibers that have lost myelin conduct nerve impulses poorly (1937)

* Lab animals are inbred to create strains susceptible to specific diseases (1933)

* Experimental Allergic Encephalomyelitis encephalomyelitis /en·ceph·a·lo·my·eli·tis/ (en-sef?ah-lo-mi?e-li´tis) inflammation of the brain and spinal cord.

acute disseminated encephalomyelitis
 (or EAE EAE

1. experimental allergic encephalomyelitis.

2. enzootic abortion of ewes.
), an MS-like disease, is caused by stimulating immune response to myelin--in inbred animals

Lymphocytes (white blood cells White blood cells
A group of several cell types that occur in the bloodstream and are essential for a properly functioning immune system.

Mentioned in: Abscess Incision & Drainage, Bone Marrow Transplantation, Complement Deficiencies
) have role in the immune response (1936)

Antibodies are made by lymphocytes called B-cells '

* A virus that infects oligodendrocyte cells of sheep and causes myelin damage is found

* Clinical Care

More 30 different treatments are tried, including: tonsil extraction, x-rays, anti-allergy injections, vasodilators Vasodilators Definition

Vasodilators are medicines that act directly on muscles in blood vessel walls to make blood vessels widen (dilate).
Purpose

Vasodilators are used to treat high blood pressure (hypertension).
 and anticoagulants Anticoagulants
Drugs that suppress, delay, or prevent blood clots. Anticoagulants are used to treat embolisms.

Mentioned in: Embolism, Heart Valve Replacement
 (to increase blood flow), psychiatry, massage, vitamins, special diets

No lasting benefits, no controlled studies

1950s to 1970s

SCIENTIFIC UNDERSTANDING

* Sodium and potassium ions found essential to nerve conduction (1950)

Tools of molecular and cellular biology developed, providing unprecedented windows into life on the cellular level

* Structure of DNA DNA: see nucleic acid.
DNA
 or deoxyribonucleic acid

One of two types of nucleic acid (the other is RNA); a complex organic compound found in all living cells and many viruses. It is the chemical substance of genes.
 revealed (1953) Family susceptibility to MS described Genes found to control "self" and "non-self" recognition (1975)

* Immune cells called T-cells react against myelin (1965)

Immune cells that "suppress" or "help" immune reactions found

Monoclonalantibodies made in lab to seek and identity specific T-cell types (1976)

Immune reactions are regulated through cytokines, made by immune cells. They include the interferons.

Blood-brain barrier stops immune cells from entering central nervous system (CNS See Continuous net settlement.

CNS

See continuous net settlement (CNS).
) (1956) Adhesion molecules involved when immune cells cross this barrier (1977)

* Search for a "triggering" virus begins (1972)

* Clinical Care

Science moves into the MS clinic

First scales to measure disability developed

First CT scans "see" MS lesions

First prevalence studies, showing gender bias and latitude effects

Study shows people with MS have higher than normal levels of antibodies against viruses

Era of controlled clinical trials in MS begins in 1960s. Early results include:

* Anti-inflammatory hormone ACTH ACTH: see adrenocorticotropic hormone.
ACTH
 in full adrenocorticotropic hormone

Polypeptide hormone made in the pituitary gland.
 speeds recovery from acute attacks (1969)

* Copolymer I--a synthetic look-a-like of myelin basic protein--"promising" in first pilot trial (1979)

1980s to 1990s

SCIENTIFIC UNDERSTANDING

* Brain cells called astrocytes astrocytes (as´trōsī´ts),
n a large, star-shaped cell found in certain tissues of the nervous system. A mass of astrocytes is called astroglia. See also astrocytoma.
 found to cause scar tissue in MS; search for agents to block scarring begins (1980)

Oglio cells can produce new myelin in adults; work to stimulate new myelin begins (1981)

Oglio cell growth factors identified (1986) Myelin is successfully transplanted from one animal to another (1989)

* Search for MS susceptibility genes: studies of twins and MS families begin (1989); studies using fast new PCR PCR polymerase chain reaction.

PCR
abbr.
polymerase chain reaction


Polymerase chain reaction (PCR) 
 technology begin (1991)

* Roles of the interferons in regulating immune response clarified (1989)

T-cell subsets that react against myelin tentatively identified (1991)

Monoclonal antibodies to adhesion molecules created; they stop immune ceils from crossing blood-brain barrier, which prevents EAE in lab animals (1992)

* Molecular mimicry theory explains how a virus could cause immune cells to attack the body's own myelin (1984)

* Clinical Care

Ideas for therapy now stem directly from new science. Many treatments prove safe enough and promising enough in lab and animal studies to test with people.

Proven treatments now control many symptoms. Many other treatments are in early clinical trials. Control of MS sought. Pilot trials are asking:

* Can antibodies that block adhesion molecules stop immune activity in the human central nervous system?

* Can antibodies against myelin (or protein fragments called peptides) block anti-myelin T-cells?

* Can oral myelin components impede or eliminate anti-myelin T-cells?

Large multi-centertrials, in progress now, are due to yield definitive results:

Beta interferon--to control relapses

Copolymer I--to control relapses

4AP--to improve nerve conduction

Before 1960, at least forty-three reports described positive results in MS treatment. But the improvements turned out to be indistinguishable from changes that would have occurred without treatment.

MS "comes and goes"---a phenomenon that has deceived many well-meaning researchers. Without controlled clinical trials, physicians treated MS with the "theory of the day" electricity in the 1860's, psychiatry in the 1930's, drugs to increase blood flow in the early 1950's.

In 1981, MS specialists formally agreed that double-blind, controlled clinical trials are the "gold standard" measurement of the effectiveness of therapies for MS.

Today, demonstrated therapies help mange mange (mānj), contagious skin disease of domestic and wild animals. The several types of mange, including follicular and sarcoptic mange, are caused by various minute parasitic mites that burrow into skin, hair follicles, or sweat glands.  symptoms such as spasticity, pain, urinary or bowel problems, and fatigue-and moderate or shorten exacerbations. Tomorrow, scientists are hopeful that treatments will be found to slow or stop the course of this formidable disorder.

Please note: The examples shown on these pages are illustrations--not a definitive list of achievements, and our dates are approximations reflecting the fact that scientific discoveries are actually acquired slowly over time, and always involve contributions from the past.
COPYRIGHT 1993 National Multiple Sclerosis Society
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 1993, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Title Annotation:multiple sclerosis
Publication:Inside MS
Date:Mar 22, 1993
Words:1017
Previous Article:Bladder blues.
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