All The Claims

What is claimed is:

1. A method for selectively stimulating proliferation and differentiation of T lymphoid cells to generate a high density of clinically relevant numbers of T lymphoid cells, comprising:
collecting material comprising body fluid or tissue containing mononuclear cells from a mammal;
treating the cells are under conditions whereby ex vivo differentiation of the cells into Th2-like or Th2 cells is induced; and
contacting, in the absence of exogenous interleukin-2, the material with two or more activating proteins specific for cell surface proteins present on cells in the material and in an amount sufficient to induce ex vivo cell expansion, whereby the cells expand to at least about 1010 cells comprising predominantly Th2 or Th2-like cells.
2. The method of claim 1, further comprising purification of the expanded cells.
3. The method of claim 1, wherein the expanded cells are specific for a defined antigen.
4. The method of claim 1, wherein the expanded cells are predominantly Th2 cells.
5. The method of claim 1, wherein the cells are activated ex vivo in the presence of IL-4 with or without the presence of anti-gamma interferon and anti-IL-12 monoclonal antibodies to cause differentiation into Th2 cells.
6. The method of claim 1, wherein the immune cells are activated ex vivo in the presence of interferon-, whereby differentiation of Th2 cells are effected.
7. The method of claim 1, wherein the proteins specific for cell surface proteins are one or more monoclonal antibodies specific for immune cell surface proteins.
8. The method of claim 7, wherein the monoclonal antibodies are specific for CD3 or CD2, combined with any combination of monoclonal antibodies specific for one or more of the following: CD4, CD8, CD11a, CD27, CD28, CD44 and CD45RO.
9. The method of claim 1, wherein cell expansion is effected in a hollow fiber bioreactor.
10. The method of claim 1, wherein the cells are expanded to an excess of 1010 cells.
11. The method of claim 4, wherein the expanded cells are purified.
12. The method of claim 1, wherein the mammal is a human.
13. The method of claim 2, wherein the mammal is a human.
14. The method of claim 7, wherein the mammal is a human.
15. The method of claim 1, wherein the expanded cells are predominantly Th2 cells, whereby the resulting population has a Th2 or Th2-like cytokine profile.
16. The method of claim 2, wherein the expanded cells are predominantly Th2 cells, whereby the resulting population has a Th2 or Th2-like cytokine profile.
17. The method of claim 7, wherein the expanded cells are predominantly Th2 cells, whereby the resulting population has a Th2 or Th2-like cytokine profile.
18. A method for generating clinically relevant cell numbers of Th2 or Th2-like T lymphoid cells, comprising:
(a) collecting material containing mononuclear T lymphoid cells from a mammal;
(b) activating the T lymphoid cells to alter their cytokine production profile by causing differentiation of the cells into Th2 or Th2-like cells; and
(c) inducing cell proliferation and expanding the cells under conditions that produce at least about 1010 cellsliter of a homogeneous population of Th2 or Th2-like T lymphoid cells.
19. The method of claim 18, wherein the T lymphoid cells with altered cytokine profile are purified.
20. The method of claim 18, wherein the T lymphoid cells with altered cytokine profile are specific for a defined antigen.
21. The method of claim 18, wherein the T lymphoid cells are activated to differentiate into Th2 cells.
22. The method of claim 18, wherein the resulting population of expanded cells includes Th2-like cells.
23. The method of claim 22, wherein the cells are activated in the presence of IL-4 anti-gamma interferon antibodies andor anti-IL-12 antibodies, whereby cells differentiate into Th2 cells
24. The method of claim 18, wherein the cells are expanded in the presence of two or more monoclonal antibodies.
25. The method of claim 24, wherein the monoclonal antibodies are specific for CD3 or CD2, combined with any combination of monoclonal antibodies specific for one or more of the following: CD4, CD8, CD11a, CD27, CD28, CD44 and CD45RO.
26. The method of claim 18, wherein the cells are expanded in a hollow fiber bioreactor.
27. The method of claim 18, wherein the cells are expanded to an excess of 109 cells.
28. The method of claim 18, wherein the cells are expanded to an excess of 1010 cells.
29. A method for generating clinically relevant numbers of regulatory T lymphoid cells for autologous cell therapy, comprising:
(a) collecting material comprising body fluid or tissue containing mononuclear cells from a mammal;
(b) treating the cells to induce differentiation of mononuclear cells into Th2 or Th2-like cells; and
(c) contacting the resulting differentiated cells with two or more activating proteins specific for cell surface proteins present on the cells in an amount sufficient to induce ex vivo cell expansion, whereby clinically relevant numbers of regulatory cells for autologous cell therapy are generated.
30. The method of claim 29, wherein cells are purified from the material.
31. The method of claim 29, wherein the treating and contacting steps occur in the absence of exogenous cytokines or the contacting step occurs in the absence of exogenous cytokines.
32. The method of claim 29, wherein the cells are specific for a selected antigen.
33. The method of claim 29, wherein the resulting cells comprise CD4 T-cells.
34. The method of claim 29, wherein the resulting cells are predominantly Th2 cells.
35. The method of claim 29, wherein the resulting cells comprise CD8 T-cells.
36. The method of claim 29, wherein at step (b) the cells are treated with IL-4 with or without anti-gamma interferon antibodies andor anti-IL-12 antibodies to cause differentiation into Th2 cells.
37. The method of claim 29, wherein the proteins specific for cell surface proteins are one or more monoclonal antibodies specific for immune cell surface proteins.
38. The method of claim 37, wherein the monoclonal antibodies are specific for CD3 or CD2, combined with any combination of monoclonal antibodies specific for one or more antigens selected from the group consisting of CD4, CD8, CD11a, CD27, CD28, CD44 and CD45RO.
39. The method of claim 29, wherein cell expansion is effected in a hollow fiber bioreactor.
40. The method of claim 29, wherein the cells are expanded to about 109 cells or greater.
41. The method of claim 29, wherein the cells are expanded to about 1010 cells or greater.
42. The method of claim 29, wherein the expanded cells are predominantly Th2 cells.
43. The method of claims 29, wherein the expanded cells are contained in a volume of one liter or less.
44. The method of claim 29, wherein the expanded cells are contained in a volume of about 500 mls or less.
45. The method of claim 29, wherein the expanded cells are contained in a volume of about 250 mls or less.
46. The method of claim 29, wherein the expanded cells are predominantly Th2-like cell, wherein:
Th2-like cells are cells that produce a majority of Th2 cytokines.
47. A method for generating clinically relevant numbers of regulatory Th2, or Th2-like lymphoid cells for autologous cell therapy, comprising:
(a) collecting material comprising body fluid or tissue containing T lymphoid cells from a mammal;
(b) treating the cells to induce differentiation of some of the mononuclear cells into Th2 or Th2-like cells, wherein Th2-like cells are cells that produce a majority of Th2 cytokines; and
(c) contacting the cells with two or more activating proteins specific for cell surface proteins present on the cells in an amount sufficient to induce ex vivo cell expansion, whereby clinically relevant numbers of Th2 or Th2-like lymphoid cells are generated.
48. The method of claim 47, wherein cells are either purified or purged from the material.
49. The method of claim 47, wherein the treating or contacting steps occur in the absence of exogenous cytokines.
50. The method of claim 47, wherein the regulatory cells are specific for a defined antigen.
51. The method of claim 47, wherein the regulatory cells are CD4 T-cells.
52. The method of claim 47, wherein the regulatory cells are CD8 T-cells.
53. The method of claim 47, wherein the cells are treated with IL-4 with or without the presence of anti-gamma interferon monoclonal antibodies andor anti-IL-12 monoclonal antibodies to cause the differentiation into Th2 cells.
54. The method of claim 47, wherein the proteins specific for cell surface proteins are one or more monoclonal antibodies specific for immune cell surface proteins.
55. The method of claim 54, wherein the monoclonal antibodies are specific for CD3 or CD2, combined with any combination of monoclonal antibodies specific for one or more of the following: CD4, CD8, CD11a, CD27, CD28, CD44 and CD45RO.
56. The method of claim 47, wherein cell expansion is effected in a hollow fiber bioreactor.
57. The method of claim 47, wherein the cells are expanded to an excess of 109 cells.
58. The method of claim 47, wherein the cells are expanded to an excess of 1010 cells.
59. The method of claim 47, wherein the expanded cells are administered to a patient.
60. The method of claims 47, wherein the expanded cells are contained in a volume of about one liter or less.
61. The method of claim 47, wherein the expanded cells are contained in a volume of about 500 mls or less.
62. The method of claim 47, wherein the expanded cells are contained in a volume about 250 mls or less.
63. The method of claim 47, wherein the expanded cells are predominantly Th2 cells.
64. The method of claim 47, wherein the expanded cells are predominantly Th2-like cells.
65. The method of claim 47, wherein the expanded cells are predominantly Th2 cells.
66. The method of claim 1, wherein the 1010 cells that are predominantly Th2 cells are produced.
67. The method of claim 66, wherein the expanded cells are administered to a patient.
68. The method of claim 1, wherein the cells are at a density of 1108 cellsml.
69. The method of claim 1, wherein density of the cells is at least 109 cellsliter.
70. The method of claim 1, wherein density of the cells is at least 1010 cellsliter.
71. A composition, comprising predominantly Th2 or Th2-like cells produced by the method of claim 1.
72. The composition of claim 71, wherein the cells are at a density of 1108 cellsml.
73. A method of treatment of diseases in which a Th1 cytokine profile predominates, comprising administering the composition of claim 71, thereby altering the ratio of Th1Th2 cell.
74. The method of claim 72, wherein the disease is a chronic inflammatory disease, chronic infectious diseases or an autoimmune disease.
75. The method of claim 74, wherein the disease is selected from the group consisting of multiple sclerosis, rheumatoid arthritis, Crohn’s Disease, autoimmune thyroid disease and inflammatory bowel disease
76. The method of claim 74, wherein the disease is selected from the group consisting of infections with human immunodeficiency virus, herpes simplex virus, cytomegalovirus or hepatovirus.
77. A composition produced by the method of claim 20.
78. A method of specific immunosuppression in organ and tissue transplant procedures or to provide immunoprotection in vaccination, comprising administering the composition of claim 20.
79. The method of claim 74, wherein the disease is rheumatoid arthritis, wherein the composition is produced by a method comprising:
collecting mononuclear cells from a rheumatoid arthritis patient;
expanding the cells under conditions whereby a composition containing an amount of Th2 cells sufficient to suppress or reduce the chronic inflammatory lesions of the arthritis; and
infusing the resulting composition of cells into the patient.
80. The method of claim 79, wherein the number Th2 cells is at least 109.
81. The method of claim 79, wherein the cells are contained in a volume of 1 liter or less.
82. The method of claim 74, wherein the disease is multiple sclerosis, and the composition is produced by a method, comprising:
collecting mononuclear cells from a multiple sclerosis patient;
expanding the cells under conditions whereby a composition containing an amount of Th2 cells sufficient to ameliorate the symptoms or retard or stop the progression of multiple sclerosis; and
infusing the resulting composition of cells into the patient.
83. The method of claim 82, wherein the number of cells is at least 109 cells.
84. The method of claim 82, wherein the cells are contained in a volume of 1 liter or less.
85. The method of claim 82, wherein the cells have a memory phenotype.
86. The method of claim 82, wherein the cells are specific for myelin or encephalitogenic epitopes of myelin antigens.
87. The method of claim 74, wherein the disease inflammatory bowel disease (IBD), and the composition is produced by a method, comprising:
collecting mononuclear cells from an IBD patient;
expanding the cells under conditions whereby a composition containing an amount of Th2 cells sufficient to ameliorate the symptoms or retard or stop the progression of the IBD; and
infusing the resulting composition of cells into the patient.
88. The method of claim 87, wherein the number of cells is at least 109 cells.
89. The method of claim 87, wherein the cells are contained in a volume of 1 liter or less.
90. The method of claim 87, wherein the disease is Crohn’s disease (CD) or ulcerative colitis (UC).
91. The method of claim 87, wherein the Th2 cells are express integrin, 4, 7.
92. A method for suppression transplant rejection, comprising:
collecting mononuclear cells from a patient prior to undergoing organ or tissue transplantation;
expanding the cells under conditions whereby a composition containing an amount of Th2 cells sufficient to prevent rejection of the transplanted organ or tissue; and
infusing the resulting composition of cells into the patient.
93. The method of claim 92, wherein the number of cells is at least 109 cells.
94. The method of claim 92, wherein the cells are contained in a volume of 1 liter or less.
95. The method of claim 92, wherein the transplanted tissue are transplanted islets of Langerhans.
96. The method of claim 92, wherein the cells are specific for the alloantigens or for an antigen unique to the transplanted tissue or organ.
97. A method for treating insulin-dependent diabetes mellitus (IDDM), comprising:
collecting mononuclear cells from a patient diagnosed with IDDM or at high risk for developing IDDM;
expanding the cells under conditions whereby a composition containing an amount of Th2 cells sufficient to prevent or retard islet destruction; and
infusing the resulting composition of cells into the patient.
98. The method of claim 97, wherein the number of cells is at least 109 cells.
99. The method of claim 97, wherein the cells are contained in a volume of 1 liter or less.
100. Cells produced by the method of claim 1 that have a CD4 phenotype.
101. Cells produced by the method of claim 1 that have a CD8 phenotype

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1.-20. (canceled)
21. A laptop computer comprising:
a computer housing including a first portion and a second portion, the first portion including a display and the second portion including a keyboard, the first portion being movable relative to the second portion to an open position;
an electro-optical sensor supported by the first portion and oriented toward a work volume above the second portion when the first portion is in the open position, the electro-optical sensor providing an output; and
a processing unit coupled to the electro-optical sensor output and adapted to determine a three-dimensional location of a portion of a person in the work volume above the second portion.
22. The laptop computer of claim 21 wherein the processing unit is adapted to determine a gesture.
23. The laptop computer of claim 21 wherein the processing unit is adapted to determine a pointing direction of a finger of the person.
24. The laptop computer of claim 21 wherein the processing unit is adapted to determine a relative location of two portions of said person.
25. The laptop computer of claim 22 wherein the processing unit is adapted to compare successive outputs of the electro-optical sensor to determine the gesture.
26. The laptop computer of claim 22 wherein the gesture includes at least one of a push gesture, a pull gesture, a grasp gesture and a pinch gesture.
27. The laptop computer of claim 21 further including a light source adapted to illuminate said portion within the work volume.
28. The laptop computer of claim 27 wherein the light source includes at least one light emitting diode.
29. The laptop computer of claim 21 wherein the electro-optical sensor includes first and second cameras.
30. The laptop computer of claim 24 wherein the first portion defines first and second apertures for the first and second cameras.
31. A computer apparatus comprising:
a laptop housing;
a display incorporated into the laptop housing;
an electro-optical sensor incorporated into the laptop housing proximate the display, the electro-optical sensor providing an output; and
a processing unit adapted to determine a three-dimensional location of a portion of a person based on the output of the electro-optical sensor, wherein the three-dimensional location of the portion of a person is used to input data into the computer apparatus.
32. The computer apparatus of claim 31 wherein the processing unit is adapted to determine a gesture.
33. The computer apparatus of claim 31 wherein the processing unit is adapted to determine a pointing direction of the person.
34. The computer apparatus of claim 31 wherein the processing unit is adapted to determine a relative location of at least two portions of the person.
35. The computer apparatus of claim 32 wherein the gesture includes at least one of a push gesture, a pull gesture, a grasp gesture and a pinch gesture.
36. The computer apparatus of claim 32 wherein the processing unit is adapted to compare successive outputs of the electro-optical sensor to determine the gesture.
37. The computer apparatus of claim 31 wherein the electro-optical sensor includes first and second cameras.
38. The computer apparatus of claim 31 wherein the display is a three-dimensional display.
39. The computer apparatus of claim 31 further including a light source incorporated into the laptop housing.
40. The computer apparatus of claim 39 wherein the light source includes at least one light emitting diode.

1. A system comprising:
a first I-Q modulator configured to modulate a first light source in response to first I and Q modulation signals;
a second I-Q modulator configured to modulate a second light source in response to second I and Q modulation signals;
a transmission signal processor configured to:
receive a data stream including data corresponding to a first data subchannel;
map said first data subchannel to a first optical transmission subchannel; and
output said first I and Q modulation signals to modulate said first light source to produce an optical transmission signal that includes wavelength components corresponding to said first optical transmission subchannel; and

a polarization multiplexer configured to receive outputs of said first and second I-Q modulators and output said optical transmission signal with first and second polarization modes.
2. The system of claim 1
wherein said transmission signal processor is further configured to:
map a second data subchannel of said data stream to a second optical transmission subchannel; and
output said second I and Q modulation signals to modulate said second light source to produce wavelength components of said optical transmission signal that correspond to said second optical transmission subchannel.
3. The system of claim 2, wherein said transmission signal processor is selectively configurable to implement different modulation protocols for said first and second transmission subchannels.
4. The system of claim 2, wherein a single laser provides both of said first and second light sources.
5. The system of claim 4, wherein said laser is a fixed-frequency optical source.
6. The system of claim 2, wherein said first data subchannel is mapped to a horizontal polarization of said optical transmission signal, and said second data subchannel is mapped to a vertical polarization of said optical transmission signal.
7. The system of claim 2, further comprising an optical receiver including an optical hybrid configured to recover I and Q signals for each of said first and second polarization modes.
8. The system of claim 2, further comprising a first optical receiver configured to recover said first data subchannel from said optical transmission signal, and a second optical receiver configured to recover said second data subchannel from said optical transmission signal.
9. The system of claim 1, further comprising an optical receiver configured to recover data corresponding to said first data subchannel from said first optical transmission subchannel.
10. The system of claim 9, wherein said optical receiver is configured to recover data from fewer than all optical transmission subchannels present on said optical transmission signal.
11. The system of claim 1, further comprising digital to analog converters configured to convert said first I and Q modulation signals to analog signals output to said first I-Q modulator.
12. A method comprising:
configuring a first I-Q modulator to modulate a first light source in response to first I and Q modulation signals and a second I-Q modulator to modulate a second light source in response to second I and Q modulation signals; and
configuring a transmission signal processor to:
receive a data stream including data corresponding to first and second data subchannels;
map said first and second data subchannels to first and second optical transmission subchannels; and
output said first and second I and Q modulation signals to modulate said first and second light sources to produce an optical transmission signal that includes wavelength components corresponding to said first and second optical transmission subchannels.
13. The method of claim 12 further comprising:
configuring a polarization multiplexer to receive outputs of said first and second I-Q modulators and output said optical transmission signal with first and second polarization modes.
14. The method of claim 13, wherein said transmission signal processor is selectively configurable to implement different modulation protocols for said first and second transmission subchannels.
15. The method of claim 13, wherein a single laser provides both of said first and second light sources.
16. The method of claim 13, wherein said first data subchannel is mapped to a horizontal polarization of said optical transmission signal, and said second data subchannel is mapped to a vertical polarization of said optical transmission signal.
17. The method of claim 13, further comprising configuring an optical receiver including an optical hybrid to recover I and Q signals for each of said first and second polarization modes.
18. The method of claim 13, further comprising configuring a first optical receiver to recover said first data subchannel from said optical transmission signal, and configuring a second optical receiver to recover said second data subchannel from said optical transmission signal.
19. The method of claim 12, further comprising configuring an optical receiver to recover data corresponding to said first data subchannel from said first optical transmission subchannel.
20. The method of claim 19, wherein said optical receiver is configured to recover data from fewer than all optical transmission subchannels present on said optical transmission signal.
21. The method of claim 12, further comprising configuring digital to analog converters to convert said first I and Q modulation signals to analog signals output to said first I-Q modulator.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. An optical pickup for recording information on an optical recording medium and retrieving information from the optical recording medium by radiating a light beam on the optical recording medium comprising:
a light source which emits the light beam;
an object lens which converges the tight beam into a convergent light beam and directs the convergent light beam to a recording layer of the optical recording medium; and
an aberration correction lens assembly between the light source and the object lens and including at least one movable lens which is movable in an optical axis direction, the aberration correction lens assembly controlling the movable lens to convert the light beam to one of a convergent light beam and a divergent light beam so as to correct spherical aberration, wherein a distance between a principal plane of the aberration correction lens assembly on a light emergent side and a principal plane of the object lens on a light incident side falls within a range determined in accordance with a numerical aperture of the object lens, a focal length of the aberration correction lens assembly on the light emergent side, and a focal length of the object lens,
wherein the distance between the principal plane of the aberration correction lens
assembly on the light emergent side and the principal plane of the object lens is determined by the following equation:
(
f
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where e2 represents the distance between the principal plane of a lens in the aberration correction lens assembly on the most light emergent side and the principal plane of the object lens, NA represents the numerical aperture of the object lens, f2 represents the focal length of the aberration correction lens assembly on the light emergent side, and f3 represents the focal length of the object lens,
wherein the numerical aperture of the object lens is not less than 0.80, and
wherein the focal length of the object lens is not greater than 2 mm.
2. The optical pickup according to claim 1, wherein the aberration correction lens assembly includes a positive lens group and a negative lens group, the movable lens included in at least one of the positive and negative lens groups, and a distance between a principal plane of the positive lens group and a principal plane of the negative lens group along the optical axis direction being changeable by the movable lens.
3. The optical pickup according to claim 2, wherein the aberration correction lens assembly comprises an expander lens assembly.
4. The optical pickup according to claim 1, wherein the movable lens comprises a collimator lens which converts the light beam emitted from the light source into a generally parallel light beam.
5. An optical pickup for recording information on a recording medium and retrieving information from the recording medium by radiating a light beam on the recording medium, comprising:
first lens means for directing a convergent light beam to a recording layer of the recording medium; and
second lens means located between a light source and the first lens means and including at least one movable lens such that the movable lens converts the light beam to one of a convergent light beam and a divergent light beam so as to correct spherical aberration,
wherein a distance between a principal plane of the second lens means on a light emergent side and a principal plane of the first lens means on a light incident side falls within a range determined in accordance with a numerical aperture of the first lens means, a focal length of the second lens means on the light emergent side, and a focal length of the first lens means,
wherein the distance between the principal plane of the second lens means on the light emergent side and the principal plane of the first lens means on the light incident side is determined by the following equation:
(
f
2

+

f
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where e2 represents the distance between the principal plane of the second lens means on the light emergent side and the principal plane of the first lens means, NA represents the numerical aperture of the first lens means, f2 represents the focal length of the second lens means on the light emergent side, and f3 represents the focal length of the first lens means,
wherein the numerical aperture of the first lens means is not less than 0.80, and
wherein the focal length of the first lens means is not greater than 2 mm.
6. The optical pickup according to claim 5, wherein the second lens means includes a positive lens group and a negative lens group, the movable lens included in at least one of the positive and negative lens groups, and a distance between a principal plane of the positive lens group and a principal plane of the negative lens group along an optical axis direction being changeable by the movable lens.
7. The optical pickup according to claim 6, wherein the second lens means comprises an expander lens assembly.
8. The optical pickup according to claim 5, wherein the movable lens comprises a collimator lens which converts the light beam emitted from the light source into a generally parallel light beam.
9. An optical pickup for recording information on a recording medium and retrieving information from the recording medium by radiating a light beam on the recording medium comprising:
a light source which emits the light beam;
an object lens which converges the light beam into a convergent light beam and directs the convergent light beam to the recording medium;
a collimator lens located between the light source and the object lens; and
a mechanism for moving at least one of the light source and the collimator lens to convert the light beam, incident on the object lens, to one of a convergent light beam and a divergent light beam so as to correct spherical aberration,
wherein a distance between a principal plane of the collimator lens on a light emergent side and a principal plane of the object lens on a light incident side falls within a range determined in accordance with a numerical aperture of the object lens, a focal length of the collimator lens on the light emergent side, and a focal length of the object lens,
wherein the distance between the principal plane of the collimator lens on the light emergent side and the principal plane of the object lens on the light incident side is determined by the following equation:
(
f
2

+

f
3
)

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where e2 represents the distance between the principal plane of the collimator lens on the light emergent side and the principal plane of the object lens, NA represents the numerical aperture of the object lens, f2 represents the focal length of the collimator lens on the light emergent side, and f3 represents the focal length of the object lens,
wherein the numerical aperture of the object lens is not less than 0.80, and
wherein the focal length of the object lens is not greater than 2 mm.
10. The optical pickup according to claim 9, wherein the collimator lens converts the light beam emitted from the light source into a generally parallel light beam.